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<h3>Job Description</h3>
Job Description
At Boston Fusion, we recognize diversity is the catalyst for limitless creativity.
 
As a Principal Research Scientist for Boston Fusion, you will have the opportunity to utilize your knowledge of scientific research and software engineering best practices to contribute and drive research efforts in development of systems core to the success of future Intelligence, Surveillance, and Reconnaissance (ISR) activities. This role will lead technical teams as a Principal Investigator, lead and contribute to proposal efforts, and collaborate with project teams to solve complex technical problems that support national security.
 
Every day, we go above and beyond to solve complex problems, making a difference for our nation. We do this by bringing together smart, curious people with diverse life experiences who collaborate creatively to achieve innovative technological breakthroughs. We are proudly building a work environment where you can bring your authentic self to work.
 
Due to the nature of our project work, we can only consider candidates with a current US Citizenship.
 Day to Day Responsibilities
 
 
<ul>
<li>Lead teams of two or more Scientists, Engineers, and Programmers, including identifying, assigning, and completing research and development tasks appropriate to each member of the team</li>
<li>Provide a strategic leadership role in working with a project / proposal team to identify the research approach, hypotheses to be tested, and program milestones to achieve all program objectives</li>
<li>Facilitate collaboration in large, complex teams to ensure resulting technology (algorithms, software, frameworks) achieves all research objectives</li>
<li>Select, improve, or design computational models</li>
<li>Identify relevant research approaches, hypotheses to be tested, and program milestones to achieve all program objectives with project and/or proposal teams</li>
<li>Provide scientific, technical and software design support to projects and proposals</li>
<li>Design statistically valid experiments to test and validate resulting computational models</li>
<li>Provide leadership and guidance in the analysis of results of the experiments using sound scientific principles</li>
<li>Design experiments to test and validate computational models</li>
<li>Establish and maintain a professional rapport with all project stakeholders (internal and external)</li>
<li>Additional project and proposal duties as assigned</li>
</ul>
 
Additional Responsibilities
<ul>
<li>Occasional travel to attend and present at customer meetings and essential industry conferences</li>
<li>Prepare technical briefing materials/summarize technical work and progress of projects</li>
<li>Collaborate with company leadership and senior technical staff to conduct proposal research and proposal writing</li>
<li>Publish technical reports based on original or improved algorithms created to solve the application challenges</li>
<li>Maintain high standards at work, continuously looking for solutions to improve processes and products</li>
<li>Develop, maintain, and strengthen partnerships with others inside and outside the organization to achieve Boston Fusion business goals</li>
<li>Demonstrate personal accountability, effective work habits, integrity, and ethical behavior that align with Boston Fusion corporate values</li>
<li>May perform other duties as required</li>
</ul>
 
This Job is Right for You if you Have:
 
<ul>
<li>Bachelor’s degree in computer science, engineering, mathematics, physics, or related field, with 15+ years of experience; Master’s degree with 13+ years of experience; PhD with 10+ years of experience</li>
<li>Excellent analytical and problem-solving skills</li>
<li>Ability to prioritize and manage time effectively</li>
<li>Excellent communication, writing and presentation skills</li>
<li>Ability to work both collaboratively and independently</li>
</ul>
 
Demonstrates strong competency in every category and a mastery of at least one category
<ul>
<li>Demonstrated competency in radar, signal processing, human-machine systems, computer vision, AI/ML, or other technical discipline</li>
<li>Experience implementing modeling and analysis techniques, including machine learning, operations research, optimization, control theory, probabilistic modeling, etc.</li>
<li>Understanding of mathematical principles which underlie these modeling methods</li>
<li>Experience in implementing algorithms in standard programming languages such as Python, Java, C++</li>
<li>Experience in using sound software development techniques, e.g., testing, documentation, source control</li>
</ul>
 
Preferred Technical Qualifications
<ul>
<li>Classical applied probabilistic, mathematical, and/or artificial intelligence methods (planning, searching, logic, uncertain knowledge, probabilistic reasoning, natural language processing)</li>
<li>Radar signal processing techniques</li>
<li>Machine learning frameworks (e.g., Scikit-learn, Tensorflow, PyTorch, Keras) and concepts (e.g., supervised, unsupervised, active, and reinforcement learning; neural networks; generative, discriminative models)</li>
</ul>
 
Preferred Domain Knowledge
<ul>
<li>6+ years of experience applying technology to US Department of Defense and/or Intelligence Community problems, including but not limited to the following: intelligence analysis, command and control, logistics, ISR, information operations, missile defense, operations in the cyber, space, or maritime domains</li>
<li>8+ years of experience in a research leadership role</li>
<li>Work Authorization/Security Clearance Requirements</li>
<li>U.S. citizenship and DoD security clearance (REQUIRED)</li>
</ul>
 
PI5a092aa8e79f-25405-36297946

Principal Research Scientist

<h3>Job Description</h3>
Job Description
Hillstar Bio is ushering in a new era in autoimmune disease treatment through precision immunology. The company selectively targets and depletes pathogenic immune cells while sparing healthy ones, offering the potential for durable relief and immune reset for patients with autoimmune conditions. Unlike traditional therapies that broadly suppress the immune system, Hillstar Bio's targeted approach addresses specific disease mechanisms by eliminating the underlying source and reducing the risks associated with chronic broad immunosuppression. 
Hillstar Bio is revolutionizing autoimmune disease treatment through a precision-driven approach that selectively depletes pathogenic cells while preserving healthy ones. This method holds the promise of providing durable relief and improving patient outcomes compared to traditional immunosuppressive therapies. Additionally, the company's versatile approach leverages tailored discovery techniques for each therapeutic, free from the constraints of traditional drug development platforms. The new funding will propel Hillstar Bio’s lead program, which specifically targets TRBV9+ T cells, into clinical trials in 2026. Initially, the focus will be on treating axial spondyloarthritis (AxSpA) and potentially other immune and inflammatory conditions associated with HLA-B27. The investment will also support the expansion of Hillstar Bio’s portfolio, which includes a variety of precision immunology therapies aimed at specific immune cell subsets across a range of autoimmune diseases. 
Hillstar Bio, a leading biotechnology company focused on developing next-generation precision immunology therapies for autoimmune diseases, announced the successful closing of a $67 million Series A financing round in March 2025. This funding was led by a syndicate of experienced investors and shareholders from the U.S., Europe, and Asia, including Droia Ventures, Frazier Life Sciences, Novo Holdings A/S, LifeArc Ventures, and Hummingbird Bioscience. Hillstar Bio is fully funded through early clinical studies to accelerate development of its TRBV9 program while expanding its pipeline of selective immune cell targeting therapies. To learn more visit <a href="http://www.hillstarbio.com" target="_blank">www.hillstarbio.com</a>
Hillstar Bio boasts a world-class team with deep expertise in antibody engineering, immunology, and clinical development. The company's approach combines cutting-edge scientific knowledge with a robust, risk-mitigating strategy, leveraging validated technologies and disease-specific biomarkers to identify the patient populations most likely to benefit from their treatments.
Job Description
Join Hillstar Bio as a Scientist/Senior Scientist Immunology overseeing the design and execution of in vitro and in vivo mechanistic, proof-of-concept and safety studies, provide scientific and technical expertise in immune cell biology, and support regulatory filing with authoring of technical reports. 
This pivotal role offers a chance to shape our company culture, make a meaningful impact on patient care, and contribute to the growth of a pioneering organization. We seek a passionate, hands-on scientist with a collaborative spirit, ready to thrive in a dynamic, close-knit team environment.
Requirements
Essential Duties and Responsibilities
<ul>
<li>Design, execute, and analyze in vitro and in vivo experiments to investigate disease-causing mechanisms and generate proof-of-concept studies. </li>
<li>Establish and validate in vitro models of autoimmune diseases; support the design and execution of in vivo experiments such as PK, tox, dosing</li>
<li>Develop and perform biochemical and biological assay (ELISA, flow cytometry, immunofluorescence, cell sorting)</li>
<li>Provide scientific guidance to external academic collaborations, vendors, CROs.</li>
<li>Assist in authoring technical reports for regulatory filing.</li>
<li>Catalyze emerging scientific breakthroughs in precision immunology into new discovery programs. </li>
<li>Play a key team role in building and fostering Hillstar’s culture and contribute to its growth.</li>
<li>Collaborate on various aspects of general business and people operations, as needed.</li>
</ul>
Qualifications
<ul>
<li>PhD in Immunology or related field.</li>
</ul>
<ul>
<li>A minimum of 2 years of experience in drug development in biotech or pharma setting, with research experience in autoimmune diseases.</li>
<li>Demonstrated experience in humoral and cell-mediated immunology, experience with B and T cell biology is highly preferred. </li>
<li>Demonstrated experience with biochemical and cell-based assays (flow cytometry, cell sorting, and microscopy is required).</li>
<li>Relevant experience is reflected by a track record of patents and high impact publications.</li>
<li>Self-motivated, collaborative, excellent time management and interpersonal skills.</li>
<li>Experience with antibody development is a plus.</li>
</ul>
Benefits
Hillstar Bio offers a competitive compensation and benefits package that includes unlimited vacation and market-leading parental leave.
Additional Information
This is a full-time position located in our Boston, MA office. Hillstar is committed to creating a diverse work culture and we are seeking individuals of all backgrounds, orientations, and identities. We are an equal opportunity employer and do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Senior Scientist Immunology

<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 Biologics Discovery Sciences group at AbbVie is seeking a highly skilled and self-motivated scientist to join a dynamic team supporting Discovery Biotherapeutics. This position will impact projects through engineering, production, and characterization of multispecific biopharmaceutical products. The ideal candidate should have extensive experience with biologics and multispecifics production platforms, analytical characterization (e.g., SEC, MS), and a proven track record implementing multispecific engineering and production strategies to advance early- and late-stage discovery programs. The ideal candidate will also have people and project management experience. The applicant should be an enthusiastic, creative scientist who will make tangible contributions to the continuous improvement and innovation within the organization.
Key Responsibilities:
<ul>
<li>Responsible for design, engineering and production of multispecific biologics to support all Abbvie therapeutic areas</li>
<li>Evaluate and integrate state-of-the-art technology to improve therapeutic production platforms, and demonstrate creative “out-of-the-box” thinking to solve difficult problems</li>
<li>Supervise 1-2 scientists, evaluate team performance, and is accountable for the effective performance of team</li>
<li>Serve as a Multispecifics Engineering representative for cross-functional teams, and contribute scientific insights into multiple projects across various therapeutic areas; recognized expert in multispecifics design and production</li>
<li>Serve as the Biologics lead on projects to coordinate activities and transitions from hit generation through candidate nomination</li>
<li>Identify and solve technical problems independently, conceive and implement innovative process research ideas</li>
<li>Ensure consistency and quality of technical reports</li>
<li>Provide project update, analysis and advice to cross-functional teams and senior management</li>
<li>Present original work internally across departments and at internal and external scientific conferences; may author or co-author peer-reviewed scientific papers or patents</li>
</ul>
Qualifications 
Qualifications:
<ul>
<li>PhD, MS, or BS degree in Biochemistry, Biochemical engineering or related disciplines with typically 4+ (PhD), 10+ (BS) or 12+ years of experience</li>
<li>Extensive experience in multispecific biologics engineering and knowledge of biologic pipeline progression from exploratory through candidate nomination</li>
<li>Extensive experience with protein, biologics, fragments, and multi-specifics design, expression and purification</li>
<li>Experience managing direct reports and providing performance evaluations and development opportunities</li>
<li>Program management experience preferred</li>
<li>Experience with CRO coordination</li>
<li>Ability to explore and develop new approaches to further advance innovative purification and screening technologies for multispecifics</li>
<li>Sound scientific understanding of current state of protein expression/separation/analytical technologies</li>
<li>Experience with in vitro analytical techniques for protein characterization (e.g. SEC, MS, DSF); experience with developability screening for multispecifics preferred</li>
<li>Strong molecular biology skills (e.g. molecular cloning)</li>
<li>Experience with sequence analysis tools (Vector NTI, Geneious, Genedata)</li>
<li>Excellent organizational skills and the ability to manage multiple projects simultaneously</li>
<li>Team player with the ability to operate in a fast-paced multi-disciplinary environment</li>
<li>Adapt to rapid changes in project priorities and timelines</li>
<li>Recognized in the scientific community through a sustained record of peer-reviewed publications and patents preferred</li>
<li>Candidate must be a goal-oriented team player with excellent verbal and written communication skills and strong can-do attitude</li>
</ul>
Key AbbVie Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable high performance.</li>
<li>Learns fast, grasps the “essence” and can change the course quickly where indicated.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality.</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>
<li>
This job is eligible to participate in our long-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 II, Multispecific Engineering

<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 DescriptionDescription:
At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively and completely eliminate the root causes of autoimmune and allergic diseases, and to achieve deep, durable responses while preserving essential immunity. We are looking for passionate individuals to join our mission to transform treatment paradigms across the spectrum of antibody-driven diseases.
 
We are looking for a self-motivated and intellectually curious Scientist/Senior Scientist to join our Biology/in vitro pharmacology group. The role will support pre-clinical efforts to characterize mechanism-of-action of therapeutics aimed at treating antibody-driven diseases. The ideal candidate is skilled lab-based in vitro biologist with a strong background in immunology and/or biologics drug discovery who can drive forward projects that serve multiple programs. 
 
Responsibilities:
<ul>
<li>Help drive multiple autoimmune programs to Development Candidate and IND</li>
<li>Design and execute in vitro experiments to support preclinical drug discovery including disease modeling, and mechanism-of-action studies to deeply characterize our molecules.</li>
<li>Collaborate with internal groups and lead study design for external CRO-based work, including biochemical analyses and in vivo studies</li>
<li>Independently develop and execute quantitative assays (ELISAs, cell proliferation assays, etc.) to support molecule progression to DC and IND.</li>
<li>Managing inventory and testing of patient samples that support multiple pre-clinical programs</li>
<li>Interpret, summarize and present research findings in internal scientific meetings as part of our collaborative learning culture.</li>
<li>Proactively review literature to bring newest scientific findings, ideas and technologies for discovery research</li>
</ul>
Requirements:
<ul>
<li>PhD in with 0-3 years, a Masters with 6+ years, or a Bachelors with 8+ years of post-graduate academic or industry experience in relevant scientific fields such as immunology, cell/molecular biology or signal transduction</li>
<li>Experience culturing and assaying human and mouse immune cells and cell lines using standard cell biology and molecular techniques (flow cytometry, ELISAs, Western Blot, PCR) is required.</li>
<li>Experience culturing primary human B cells is a plus, as is experience designing viral vectors to express antigen receptors (particularly BCRs) and characterizing downstream signaling. </li>
<li>Ability to work within a dynamic, matrixed environment.</li>
<li>Excellent written and verbal communication skills, as well as strong organizational and problem-solving abilities.</li>
</ul>
Merida Biosciences is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
 
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.

Scientist/Senior Scientist, Biology

<h3>Job Description</h3>
Job DescriptionPrincipal Scientist, Translational Sciences Job summary: PharmaEssentia Innovation Research Center (PIRC) is seeking a highly motivated principal scientist to join our Translational Sciences team and contribute to the development of first-in-class and best-in-class biotherapeutics, including cytokines, antibodies, and antibody-drug-conjugates. &nbsp;The successful candidate will contribute to the design, execution, and interpretation of translational biomarker and mechanism of action (MOA) studies to support the development and regulatory approval of novel therapeutics as they transition from late discovery into first in human clinical trials and beyond.&nbsp; You will also drive translational and early clinical activities aimed at maximizing the potential of BESREMI, PharmaEssentia’s marketed drug for the treatment of myeloproliferative neoplasms, including indication expansion and novel combinations. &nbsp;To this end, you will work cross-functionally with clinical development, clinical operations, regulatory affairs as well as with academic investigators and clinical CROs to explore new applications for BESREMi.&nbsp; Additionally, you will provide scientific leadership, mentorship, and cross-functional collaboration within the Translational Sciences team and across other departments. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), will build upon our invention and discovery-based innovation efforts originally established in Taiwan that led to a transformative advancement for treating polycythemia vera (one of the myeloid proliferative neoplasms). At PIRC, we aim to expand our current expertise in related therapeutic areas and identify novel therapeutic approaches in early to mid-stage discovery and development. Data scientists will leverage artificial intelligence and machine learning to inform new target and indication selection. The company is also recruiting for talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs leveraging disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. Summary of Key Responsibilities: &nbsp;
<ul>
<li>Further Exploration of BESREMi: Collaborate with clinical development to further explore the potential of BESREMi in MPN and other areas of Oncology. Conduct translational studies internally or externally via CROs, and drive investigator-initiated trials (IITs) or company sponsored clinical trials to maximize the clinical potential of BESREMi. </li>
<li>Study Design and Execution: Lead the design, planning, and execution of translational studies in indication-relevant animal models and primary human cellular and tissue systems to identify and validate biomarkers and explore drug candidate mechanism of action. &nbsp;Collaborate with cross-functional teams to ensure alignment with discovery and development goals as well as regulatory requirements.</li>
<li>Data Analysis and Interpretation: Oversee the analysis, interpretation, and reporting of in vitro and in vivo pharmacology/translational biomarker data, including pharmacokinetic and pharmacodynamic parameters, exposure-response relationships, and safety/tolerability profiles. Provide scientific insights to inform decision-making and optimize study outcomes.</li>
<li>Drug Development Strategy: Contribute to the development and implementation of clinical pharmacology strategies to support the progression of investigational drugs through all phases of clinical development. Generate scientific rationale for dose selection, formulation optimization, and therapeutic target validation.</li>
<li>Scientific Leadership: Serve as a subject matter expert in translational biomarkers, target biology and candidate therapeutic mechanism of action, providing guidance and mentorship to junior scientists, clinicians, and project teams. Contribute to the scientific literature through publications, presentations, and participation in professional conferences and working groups.</li>
<li>Cross-Functional Collaboration: Collaborate closely with colleagues in data sciences, biologics, immunology/pharmacology, clinical development, clinical operations and regulatory affairs to integrate translational biomarker and mechanism of action insights into overall drug development strategies. Foster a culture of scientific excellence, innovation, and collaboration. </li>
<li>Regulatory Interaction: Work with regulatory affairs and CROs to support the preparation and review of regulatory submissions, including investigational new drug (IND) applications, biologics license applications (BLA), and marketing authorization applications (MAA). Address inquiries and provide scientific justifications for study designs, endpoints, and data analyses.</li>
</ul>
 Qualifications: &nbsp;
<ul>
<li>M.D or Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>8+ years’ experience in the pharmaceutical or biotechnology industries, including a proven track record of leadership and scientific achievement in translational sciences.</li>
<li>Expertise in in vivo model design and biomarker discovery, both internally and via CROs and academic collaborations. </li>
<li>Experience with primary human cellular/tissue-based assays to guide/inform indication selection, biomarker discovery and mechanism-of-action.</li>
<li>Experience with immuno-oncology and autoimmune disease/chronic inflammation targets and associated in vitro and in vivo models.</li>
<li>Experience in clinical trial design and/or clinical operations in either company-sponsored, or IIT clinical trials. </li>
<li>Experience working closely with academic collaborators and managing all aspects of sponsored research agreements or IITs.</li>
<li>Strong analytical skills, with proficiency in pharmacokinetic/pharmacodynamic software (e.g., NONMEM, Phoenix WinNonlin, R) is preferred.</li>
<li>Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to diverse audiences.</li>
<li>Demonstrated leadership capabilities, including the ability to mentor and develop talent, foster teamwork, and drive results in a dynamic environment.</li>
</ul>
 Conclusion: As a Principal Scientist in Translational Sciences, you will play a pivotal role in advancing the understanding of drug pharmacology and contributing to the development of innovative therapeutics to address unmet medical needs. Your scientific expertise, leadership skills, and collaborative approach will be critical for driving drug development programs forward, maximizing the potential of BESREMi and ultimately improving patient outcomes at PIRC. EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies.
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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Principal Scientist, Translational Sciences

<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

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