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<h3>Job Description</h3>
Job Description
Lantheus is headquartered in Bedford, Massachusetts with offices in New Jersey, Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has helped physicians enhance patient care with its broad product portfolio. 
Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostics, targeted therapeutics, and artificial intelligence (AI) solutions that empower clinicians to find, fight and follow disease. At Lantheus our purpose and values guide our behaviors in all interactions and play a vital role in creating a dynamic environment that contributes to our success. Every employee is crucial to our success; we respect one another and act as one knowing that someone’s health is in our hands. We believe in helping people be their best and are seeking to bring together a diverse group of individuals with different viewpoints and skill sets to be a part of a productive and inclusive team. 
Position Summary
Operates with a high degree of independence and is adept at conceptually outlining development, qualification, and life-cycle management studies with a focus on process analytical concepts to monitor and control critical steps in the manufacturing process of radiopharmaceuticals, ensuring consistent quality and safety meet current regulatory requirements on radiopharmaceutical drug products. Drives development and validation of new and improved radiochemical process controls in commercial processes; implements analytical methods and/or physicochemical characterizations in support of process development; radiolabeling processes and detection; and/or technology transfer to Contract Organizations. These efforts support the economical, efficient, and safe manufacture of radiolabeled precursors, bulk drug substances, and/or drug products. Lead PET CMO analytical operations and execution from late-stage development through site qualification. Engages in the development of complex strategies and testing requiring implementation of sophisticated, specialized scientific knowledge and advanced lab techniques, with latitude for independent judgment, decisions, and action. Radiopharmaceutical experience is preferred.
Essential Functions
<ul>
<li>Plans and drives multiple projects, requiring initiative and innovation, within Lantheus’ Quality system and governing regulations. Works on complex problems of diverse scope while serving as a technical analytical SME. Identifies, analyzes, and interprets project results. Evaluates results and examines implications to program.</li>
<li>Participate in technical troubleshooting sessions for processes and products manufactured in-house and at CMOs as needed and in investigating atypical/OOS results.</li>
<li>Performs routine laboratory, including working with radioactive materials, or oversees these actions at PET CMOs. Demonstrates ability to follow SOPs and Lantheus’ procedures as written. Tracks laboratory supplies and replenishes when needed. Maintains laboratory notebook, record keeping, and laboratory safety in accordance to common industry GLPs and Lantheus’, or CMO site, procedures.</li>
<li>Exhibits an increased understanding of radiochemistry, its regulations, stays aware of new scientific developments, and is able to incorporate these into their development/qualification activities.</li>
<li>Communicates scientific ideas and information in an appropriate and timely manner. Employs active listening skills to maintain clear communication to others. </li>
<li>Provides technical support to further program and Qualification activities at CMO/CROs; Authors technical transfer protocols and ensure acquired results are collected and documented according to cGMPs; Assists in completion of close-out reports and appropriate Change Controls. </li>
<li>Shows the ability and willingness to continually enhance functional and technical expertise. Assesses own strengths/ needs and learns from experience and feedback in order to continually enhance the level of functional and technical expertise. Takes action on developmental opportunities.</li>
<li>Accurately documents results in established formats. Able to write basic reports clearly and succinctly. Prepares written reports on all phases of laboratory and/or field experimental work. Presents results to colleagues at scientific meetings and to multidisciplinary audiences in program meetings. Writes comprehensive reports based on literature, lab and field data.</li>
<li>Maintains current knowledge of, and ensure all work activities are conducted in compliance with the full range of related internal and external systems, technology, regulatory requirements and related policies and procedures. Follows procedures to support intellectual property protection. May be responsible for preparing and defending patent disclosures and applications.</li>
<li>Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety &amp; environmental hazards.</li>
<li>Actively demonstrates the Lantheus values of Helping people be their best; Respect one another and act as one; Learn, adapt, and win; Know someone’s health is in our hands; and Own the solution and make it happen.</li>
</ul>
Typical Minimum Skills and Experience and Education 
<ul>
<li>Degree in Chemistry, Engineering, or related discipline or equivalent relevant industry experience.</li>
<li>Requires a minimum of a Ph.D. degree and 5+ years relevant industry work experience or a M.S. degree and 8+ years relevant work experience or a B.S. degree and 10+ years relevant industry work experience.</li>
<li>Scientific knowledge and experience in the technical aspects of radioanalytical chemistry and radiopharmaceutical process development and expertise in GMP documentation requirements with a working understanding of 21CFR 212 regulatory guidelines.</li>
<li>Previous experience working with radiopharmaceuticals and CMOs strongly preferred.</li>
</ul>
Other Requirements
<ul>
<li>Exceptional knowledge of scientific field of specialization. Familiar with Code of Federal Regulations parts 210 and 211 and supporting regulatory inspections.</li>
<li>Demonstrated skills in leading projects on an assigned team.</li>
<li>Able to properly handle and minimize exposure to potentially hazardous chemical, or radiological materials. Required to follow all safety procedures, and use personal and protective equipment provided.</li>
<li>Demonstrated competence in the design and documentation of complex experiments focused on a specific topic. Expanded scope to include multiple related questions for a given program.</li>
<li>Routine and or frequent lifting, with reasonable accommodations.</li>
<li>Demonstrated ability to effectively communicate ideas and information, both in oral and written form.</li>
<li>Travel (including international) is highly anticipated.</li>
</ul>
Lantheus is an equal opportunity employer that provides a workplace free from discrimination. All qualified applicants and employees are considered without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any other characteristic protected by law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition team at <a href="mailto:talentacquisition@lantheus.com" target="_blank">talentacquisition@lantheus.com</a>.

Senior Scientist II PET Analytical Development

<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 
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 Bioinformatics for Immunology, Genetics, and Genomic Sciences group in the Genomics Research Center (GRC) at AbbVie is seeking a highly motivated and experienced AI/ML leader to transform our drug discovery and development through cutting-edge method and technology innovation. AbbVie’s GRC is a center of excellence for bioinformatics, functional genomics, human genetics, and pharmacogenomics. The GRC collaborates across R&amp;D, supporting both discovery research and clinical development, while integrating with process sciences, search and evaluation initiatives, and corporate strategic planning.
This position will be based in Cambridge, Massachusetts (hybrid). The candidate will lead a team of computational biologists and AI/ML experts focused on developing computational innovation to accelerate drug discovery and development across therapeutic and functional areas such as immunology, ophthalmology, aesthetics, specialty medicine, genetic medicine, process development, novel technologies, and human genetics. The successful applicant will identify opportunities and implement innovative solutions that address critical challenges in forward and reverse translation, biomarker discovery, mechanistic characterization, and therapeutic development optimization, while effectively communicating insights to key internal teams and external partners. In addition, the candidate will contribute to presentations at scientific conferences and publications of translational findings in peer reviewed journals, new drug applications and regulatory filings.
Key Responsibilities:
· Lead a diverse team of up to 10 FTEs specializing in computational method and novel technology innovation across AbbVie’s therapeutic and functional areas.
· Design and implement advanced AI/ML algorithms tailored to tackling complex problems across the drug development pipeline, including target discovery, translational research, biomarker development, patient stratification, therapeutic design, manufacturing science, and clinical trial optimization.
· Identify, evaluate, and implement emerging AI/ML methodologies, including state-of-the-art Generative AI, to deliver measurable impact on pipeline productivity and success.
· Act as the AI/ML expert in program teams, providing guidance and suggestions on cross-functional innovation projects.
· Develop and implement analytical approaches and best practices for novel technologies such as spatial transcriptomics, long-read sequencing, and CRISPR with strategic partners.
· Mentor leaders, emerging scientists and build capabilities, fostering an environment of scientific excellence and continuous growth.
· Communicate analytical approaches and results effectively to scientific and technical audiences.
· Provide expertise and technical consultation for external collaborations/partnerships in academia and industry.
Qualifications 
Basic Qualifications:&nbsp;
· PhD. in bioinformatics, statistics, mathematics, computer science, computational biology, genomics, or a related field with 8+ years industry/academic experience.
· Or master’s degree with 15+ years of relevant experience.
· 3+ years of experience managing direct reports.
· 5+ years of hands-on experience in analyzing and integrating multi-omics data (e.g., bulk and single-cell RNA-seq, proteomics, genetics, epigenetics data).
· 3+ years of hands-on experience developing novel methods including AI and ML approaches.
· Highly proficient with statistical and programing languages (R, Python), Unix/Linux and cloud computing environment.
Preferred Qualifications:
· At least 3 years of experience managing teams, including managing managers with direct reports, and setting strategic goals for their teams within a highly matrixed organization.
· Deep understanding of human disease biology across various therapeutic areas such as immunology, aesthetics, and ophthalmology.
· Experience applying advanced computational modeling and AI/ML approaches to optimize therapeutic protein design, enhance production efficiency, and accelerate genetic medicine development.
· Expertise in predictive modeling, quantitative data analysis, and novel method development leveraging multi-modal preclinical, clinical, and real-world data.
· Experience with optimizing and fine-tuning foundation models, and applying LLM, Generative AI, and Agentic AI frameworks to biological questions.
· Experience with multi-omics data integration and with novel technologies such as spatial transcriptomics, Perturb-seq, CRISPR, long-read sequencing, etc.
· Demonstrate strong communication skills that allow you to effectively communicate complex technical concepts to diverse audiences and scientific leadership.
· Collaborative and self-motivated, able to manage multiple objectives and adapt to changing priorities.
· Strong track record of publications and/or patents in this space.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Principal Research Scientist, Method and Technology Advancements Lead

<h3>Job Description</h3>
Job Description
Biocytogen Boston Corp is seeking a highly motivated and versatile Pharmacology Scientist to support both in vivo and in vitro preclinical research services in the fields of immunology, immuno-oncology, metabolic disease and neurology. This role is ideal for candidates with broad expertise in pharmacological studies, disease model development, and cell-based assays, who are passionate about evaluating novel therapeutic agents for clients. 
The successful candidate will be a critical member of our fast-paced and expanding CRO team, actively engaging in both hands-on experimental work and strategic project management to support biotech and pharmaceutical partners
Key Responsibilities
In Vivo Pharmacology
<ul>
<li>Design and develop animal models, execute in vivo experiments to evaluate the biological efficacy of novel therapeutic agents.</li>
<li>Independently lead in vivo service projects and preclinical studies, acting as Project Manager or Study Director.</li>
<li>Perform animal handling, tumor inoculation, drug administration via multiple routes, blood and tissue collection, tumor measurements, and PK/PD studies.</li>
<li>Design and execute internal model-building projects and characterize various humanized mouse models.</li>
<li>Provide troubleshooting support and technical guidance to junior associates.</li>
<li>Collaborate closely with the BD/Sales team for client project planning and technical discussions.</li>
<li>Present project results to clients and internal stakeholders; prepare scientific reports and summaries.</li>
<li>Mentor and facilitate the growth of junior research associates.</li>
</ul>
In Vitro and Ex Vivo Pharmacology
<ul>
<li>Independently develop, validate, and perform a broad range of in vitro and ex vivo assays including:</li>
<ul>
<li>Immune cell profiling from blood and tissues.</li>
<li>Functional assays using primary cells (T cells, NK cells, macrophages).</li>
<li>Cytokine profiling, cytotoxicity, and apoptosis assays.</li>
</ul>
<li>Develop new assay technologies by researching scientific literature and adapting methodologies from collaborations and other internal teams.</li>
<li>Perform flow cytometry (FACS), ELISA, Western blot, qRT-PCR, and multiplex cytokine analyses.</li>
<li>Contribute to the design and support of in vivo pharmacology studies from an in vitro perspective.</li>
<li>Present research findings at internal meetings and contribute to external scientific discussions.</li>
</ul>
Requirements
<ul>
<li>PhD in pharmacology, immunology, cancer biology, or related biomedical field.</li>
<li>Extensive hands-on experience in animal models and preclinical in vivo pharmacology.</li>
<li>Proven skills in cell-based immunological assays including T cell activation, NK cell-mediated cytotoxicity, and macrophage functional assays.</li>
<li>Proficiency in PK/PD model establishment and analysis.</li>
<li>Expertise in flow cytometry, cytokine profiling (ELISA, qRT-PCR, multiplex assays), and immune cell isolation from tissues.</li>
<li>Experience with surgical procedures in rodents is highly desirable </li>
<li>Cross-functional knowledge across therapeutic areas is a plus.</li>
<li>Strong communication, organizational, and team collaboration skills with the ability to prioritize in a fast-paced environment.</li>
<li>Demonstrated ability to independently manage projects and work with cross-functional teams.</li>
</ul>
Benefits
<ul>
<li>Medical Insurance </li>
<li>Dental Insurance </li>
<li>Vision Insurance </li>
<li>Health Reimbursement Accounts </li>
<li>Life and AD&amp;D Insurance </li>
<li>Short &amp; Long Term Disability Insurance </li>
<li>401K with Company Match</li>
<li>Paid Time Off</li>
<li>Paid Sick Days &amp; Holidays </li>
</ul>
BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one’s qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Scientist/Senior Scientist for Pharmacology

<h3>Job Description</h3>
Job DescriptionDEKA Research &amp; Development has an immediate opening for a Biocompatibility &amp; Toxicology Senior Scientist to join our team focused on medical device and combination product development. The individual in this role will work directly with Research &amp; Development, Regulatory &amp; Clinical Affairs and Quality Engineering to formulate and execute biocompatibility and toxicological evaluation strategies that support development objectives and world-wide regulatory approvals.&nbsp; How you will make a difference as a&nbsp;Biocompatibility &amp; Toxicology Senior Scientist:
<ul>
<li>Work in close association with customers and development teams to define and execute biocompatibility/toxicology evaluations, including establishing requirements for biological safety of medical devices and combination products</li>
<li>Lead the preparation and conduct of biocompatibility/toxicology test programs</li>
<li>Lead interactions with external consultants and contract laboratories including in-person meetings, teleconferences, and other communications as needed to support program objectives</li>
<li>Develop and deploy mechanisms to continually maintain state of the art knowledge and understanding related to biocompatibility and toxicological safety of medical devices, including relevant standards and test methods.&nbsp; Insure processes and procedures maximize resource efficiency and minimize time to market</li>
<li>Insure the organization stays up to date on global regulatory changes to medical device biocompatibility standards and requirements through monitoring regulatory authority and industry resources</li>
<li>Coach and mentor internal and external partners on effective strategies and tactics</li>
<li>Interface with customers on biocompatibility and toxicology issues</li>
</ul>
Skills you will need to be successful:
<ul>
<li>MS in a technically related field (toxicology, materials science, chemical engineering, biomedical engineering or related).</li>
<li>Minimum of 7 years direct work experience in a medical device and/or combination product development role with demonstrated success in planning and conducting biocompatibility and toxicological evaluations</li>
<li>Expertise in U.S. and international medical device biocompatibility requirements including ISO 10993 standards, Good Laboratory Practices, and guidance from regulatory authorities</li>
<li>Demonstrated practical knowledge of the laboratory methods and analytical techniques associated with medical device and/or combination product biocompatibility and chemical characterization evaluations</li>
<li>Demonstrated ability to establish consensus and work collaboratively across functions and development teams</li>
<li>Excellent written and verbal communication skills including the ability to effectively communicate at all levels of the organization and with external partners</li>
</ul>
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
 &nbsp;
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Biocompatibility & Toxicology Senior Scientist

<h3>Job Description</h3>
Job DescriptionDescription Verdox, Inc. is dedicated to reversing climate change through the development and deployment of advanced technology.&nbsp; The company’s proprietary electro-swing process, developed at MIT, enables carbon dioxide and other acid gasses to be captured with up to 80% less energy and 70% less cost than conventional approaches.&nbsp; Verdox is backed by institutional investors and based in Boston. Verdox seeks a Materials Scientist/Engineer to join our R&amp;D team.&nbsp; This position reports to the Formulation Scientist. Key Responsibilities
<ul>
<li> Iteratively design, develop and execute novel and scalable formulations guided by materials understanding, structure-property relationships, and functional data</li>
<li> Build structure/property correlations with functional data and materials properties, to guide innovation</li>
<li> Develop and execute scalable coating techniques towards the continuous manufacturing of large-area conductive coatings </li>
</ul>
 Skills Knowledge and Expertise
<ul>
<li> Ph.D. in Polymer Science and Engineering, Materials Science and Engineering, Chemistry, Chemical Engineering, with at least 2-5 years of industry experience</li>
<li> Deep understanding of polymer structure/property relationships and behavior in solution and solid state</li>
<li> Basic understanding of electrochemistry, electronic and ionically conducting materials is highly desirable</li>
<li> Proficiency in polymer characterization (solution, solid state) is required, and expertise in characterization of porous materials is highly desirable</li>
<li> Demonstrated track record of interdisciplinary research</li>
<li> Strong oral and written communication skills</li>
<li> Keen attention to detail</li>
<li> Background in data analysis and statistics strongly desirable</li>
<li> Comfortable working in an evolutionary and dynamic startup environment </li>
</ul>

Materials Scientist/Engineer

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
This position performs routine testing using various chemistry techniques within the pharmaceutical industry. We seek an experienced professional who can make an immediate impact.
Responsibilities
<ul>
<li>Conduct routine testing or other analysis in a specific group or department setting.</li>
<li>Perform advanced or critical testing as required.</li>
<li>Operate specialized equipment or conduct specialized skill testing.</li>
<li>Apply working knowledge of raw materials testing and release.</li>
<li>Utilize instruments such as HPLC, GC, and ICP.</li>
<li>Lead investigation activities.</li>
<li>Ensure compliance with all data integrity and cGMP practices, procedures, and expectations.</li>
<li>Maintain compliance with all good documentation practices.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, GC, ICP, and GC-MS.</li>
<li>Experience in quality control and wet chemistry.</li>
<li>Knowledge of pharmaceutical raw materials and data entry.</li>
<li>Analytical chemistry expertise.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>1-3 years of experience in the industry for Chemist I positions; co-op experience in a cGMP pharmaceutical manufacturing setting is acceptable.</li>
<li>3-5 years of industry experience for Chemist II positions.</li>
</ul>
Work Environment
Work within a small, collaborative team of 15 people in quality, with cross-departmental collaboration. The position operates on the first shift, Monday through Friday, from 8:00 AM to 5:00 PM. The main site for product testing is in Fall River, with a focus on expanding the product line, particularly inhalants.
Relocation Bonus
Up to 6K for relocation bonus offered 
Pay and Benefits
The pay range for this position is $65000.00 - $80000.00/yr.
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 Fall River,MA.
Application Deadline
This position is anticipated to close on Aug 11, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
We are seeking an experienced and highly motivated in vivo biologist to join our Circuit Biology team within Discovery Psychiatry. The successful candidate will play a key role in facilitating insights of circuit dysfunction in psychiatric disorders and treatment. This is an excellent opportunity to work at the forefront of psychiatry drug discovery research, contributing to target validation and compound profiling studies within a dynamic and collaborative team. &nbsp;
Key Responsibilities
<ul>
<li>Independently conceive, execute, and communicate original technical ideas and novel multi-disciplinary research that achieves project and area goals.</li>
<li>Drive internal in vivo rodent electroencephalography (EEG) efforts by developing and optimizing recording strategies</li>
<li>Develop and maintain in vivo behavior and EEG technology, methodology, and utility in psychiatric drug discovery.</li>
<li>Generate, through lab-based activities EEG and behavioral endpoints to support projects</li>
<li>Ensure alignment of efforts with the broader goals of cross-functional teams</li>
<li>Present findings to internal teams and external collaborators or conferences</li>
<li>Contribute to strategic decision-making in psychiatry drug discovery</li>
<li>Provide scientific guidance and training to junior scientists and research associates</li>
</ul>
Qualifications 
Required Qualifications
<ul>
<li>Bachelor’s Degree or equivalent education and typically, 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no experience necessary.</li>
<li>Extensive experience in rodent EEG surgical techniques, recordings, and analyses.</li>
<li>Demonstrated expertise in the design and execution of hypothesis-driven studies related to synaptic and circuit function</li>
<li>Ability to process and interpret large datasets using appropriate software tools</li>
<li>Strong ability to work in cross-functional teams and effectively communicate scientific finding</li>
</ul>
<ul>
<li>Desired Qualifications</li>
<li>Previous industry experience within early discovery, preferably within psychiatry research</li>
<li>Expertise in rodent behavioral models and preclinical models for anxiety and depressive disorders, and/or schizophrenia</li>
<li>Track record of impactful publications&nbsp;</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, In Vivo Electrophysiology

<h3>Job Description</h3>
Job DescriptionBiological Scientist (Marine Biologist or Fisheries Scientist)Population Biology Branch (PBB)Falmouth, MA (WHOI); Pocasset, MA; and Narragansett, RI
This role supports more advanced biological research and technical responsibilities for the Northeast Fisheries Science Center (NEFSC) 
Join @Orchard in delivering mission-critical scientific support to the Northeast Fisheries Science Center (NEFSC) and its Population Biology Branch (PBB). This role places you at the intersection of biological research, laboratory analysis, and fieldwork, contributing to NOAA’s long-term commitment to sustainable marine resource management.
The PBB plays a vital role in conducting age, growth, and reproductive studies that inform fish stock assessments across the Northwest Atlantic. This opportunity offers hands-on engagement in specimen analysis, oceanographic surveys, and data-driven fisheries science.
@Orchard is seeking a Marine Biologist / Fisheries Scientist to support NEFSC’s research programs. In this role, you’ll collect and process biological samples, conduct histological and morphological analysis, and contribute to research cruise operations and database-driven scientific reporting.
You’ll collaborate with federal scientists, research staff, and field technicians in both lab and sea environments. Suppose you’re experienced in fisheries sampling, biological data analysis, and ready to contribute to meaningful marine research. In that case, this position offers a unique opportunity to deepen your expertise and make a meaningful impact.
Key Responsibilities
As a Biological Science Support team member, your key responsibilities include:
<ul>
<li>Collecting, sorting, identifying, and preserving biological samples and data as required.</li>
<li>Maintaining or continuing to process biological samples and data in the laboratory using routine methods.</li>
<li>Entering data and reporting to the Federal Program Lead regarding progress.</li>
<li>Participating in resource survey cruises once to up to four times per year (5-50 days per year) to assist in the collection of oceanographic and biological samples and data. In the laboratory, they shall assist in the processing of biological specimens.</li>
<li>Assisting in the use of equipment, instruments, or software to carry out standardized procedures and computations of varying complexity, and including basic, descriptive data analysis and regular communications of findings, including written summaries.</li>
<li>Providing technical support for oceanographic and fisheries sampling including assistance with finfish, elasmobranch, and invertebrate sampling; associated biological, habitat, and oceanographic sampling; supply and equipment preparation; data entry, quality assurance and control; laboratory experiments on finfish; age, reproduction, and food habits processing; fostering a safe work environment and effectively using information technology resources.</li>
<li>Performing special tasks regarding ensuring data quality and providing periodic written progress reports.</li>
<li>Participating in task/project-specific workshops, scientific meetings, and outreach events.</li>
<li>Conducting special projects regarding accessing data files, including from relational databases, analyzing histology preparations of fish gonads, and performing preliminary analyses.</li>
<li>Conducting limited professional assignments under periodic technical supervision on all phases of assignments.</li>
<li>Applying established methods, tests, procedures, and techniques, and recording actions and results.</li>
<li>Assisting with database maintenance, queries, and summaries; preparation of graphics and support for scientific reports and documents.</li>
<li>Participating in task/project-specific workshops, scientific meetings, and outreach events.</li>
</ul>
Required Experience and Qualifications:
To be successful in this role, candidates must meet the following qualifications:
<ul>
<li>Bachelor’s degree with 1-2 years’ experience or a Master’s degree</li>
<li>Experience in the identification of finfish, elasmobranchs, shellfish, and other invertebrate species commonly encountered along the Atlantic coast from Nova Scotia to Cape Hatteras</li>
<li>Demonstrated experience relevant to project-specific interests, including interpreting samples and data of:</li>
</ul>
<ul>
<ul>
<li>fish hard parts, such as otoliths or vertebrae, for ageing,</li>
</ul>
</ul>
<ul>
<ul>
<li>gonads, including maturity classification, histological methods, and fecundity</li>
</ul>
</ul>
<ul>
<ul>
<li>stomach contents, specifically to identify partially or well-digested prey</li>
</ul>
</ul>
<ul>
<li>Demonstrated experience with microscopes, image analysis systems (Image J), or electronic data entry systems.</li>
<li>Demonstrated experience at sea for more than one week at a time.</li>
<li>Demonstrated experience dissecting fish or working with live fish in aquaria.</li>
<li>Demonstrated experience with personal computers using word processing software, spreadsheets, and email.</li>
<li>Demonstrated experience with database management, including relational databases, producing data summaries and reporting (Oracle, R).</li>
<li>Basic statistical knowledge, such as a univariate, parametric statistics course.</li>
<li>Demonstrated experience collaborating on peer-reviewed scientific presentations and publications. </li>
</ul>
Essential Conditions of Employment
<ul>
<li>Sea-Readiness: Work at sea or in the laboratory may occasionally involve extended hours or weekends</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>.

Biological Scientist (Marine/Fisheries Science)

<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>.

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