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About the Role We are seeking a highly motivated Research Scientist to support cutting-edge work at the intersection of AI, machine learning, and biologics discovery. This role focuses on building scalable, data-driven modeling frameworks to accelerate therapeutic design across oligonucleotides and biologic modalities. You will play a key role in advancing AI/ML-assisted discovery pipelines, helping drive innovation in sequence-based modeling, antibody design, and next-generation therapeutics. Location: Open to Remote, within 1 hour of the Cambridge, MA 02142. What You’ll Do • Develop and implement advanced AI/ML models for antibody discovery, including generative protein design and protein language models, • Build and scale machine learning approaches for multi-objective optimization across biologic modalities, • Design sequence-aware predictive models to support oligonucleotide therapeutic development, including exon skipping response, • Create end-to-end computational frameworks covering data ingestion, feature engineering, model training, validation, and deployment, • Curate and integrate diverse datasets, including literature-based and experimental data, • Define and engineer key biological features such as sequence motifs, thermodynamics, and structural attributes, • Establish model benchmarks and collaborate with experimental teams to validate predictions, • Evaluate and integrate new tools and technologies to enhance modeling workflows, • Maintain clean, well-documented codebases and provide guidance to cross-functional teams What We’re Looking For • PhD in Computational Biology, Computational Chemistry, Machine Learning, Biomedical Engineering, or a related field, • 3+ years of relevant experience in industry or highly applicable post-PhD academic research, • Strong background in oligonucleotide chemistry and/or antibody design and characterization, • Experience modeling antibody-antigen interactions, including sequence and structural analysis, • Hands-on expertise with machine learning and deep learning methods such as RNNs, GNNs, Transformers, and generative models, • Proficiency in Python, R, and SQL, along with frameworks like PyTorch, TensorFlow, scikit-learn, or JAX, • Experience working with DNA, RNA, and protein modeling, including structure prediction and design, • Familiarity with cloud platforms, large-scale computing, and data infrastructure tools such as AWS, Docker, GitHub, or GitLab, • Strong communication skills and ability to collaborate across multidisciplinary teams Nice to Have • Experience working in cross-modality therapeutic design (e.g., biologics and oligonucleotides), • Exposure to production-level ML systems and scalable pipelines Why Join • Work on impactful, next-generation therapeutic technologies, • Collaborate with a highly interdisciplinary team of scientists and engineers, • Opportunity to contribute to innovative AI-driven drug discovery programs, • Flexible consideration for strong candidates from academic backgrounds Interested? Apply now to learn more.

Salary range: 60k - 80k Title: Operations Associate, Facilities Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess’ patch combines room temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. Research & development at Vaxess is cross-disciplinary, integrating mechanical, industrial, biomedical, and chemical engineering with chemistry, biology, and human factors to address important unmet medical needs. We are seeking a talented, collaborative, and highly motivated engineer to join our growing team. This role offers a unique opportunity to build manufacturing capacity from the ground up to bring innovative technology to the global vaccine and therapeutic market. Vaxess Manufacturing Tour Responsibilities • Provide support for the overall lab environment, ensuring proper functioning of utilities, lab equipment and life, • safety systems, • Perform facility & safety inspections including chemical, biological and universal waste consolidation, • Perform equipment installations, qualifications and calibrations for lab & facility equipment/casework, • Provide support to various facilities administration duties including but not limited to external vendor, • coordination, landlord services, HVAC, plumbing, etc., • Provide support to consumable, chemical and off-site storage inventories, • Collaborate closely with cross-functional teams to support product development and manufacturing activities, • Maintain necessary certifications DOT, RCRA, Bloodborne Pathogens, etc. Qualifications • 2-4 years’ experience as on-site technician working in an industrial R&D, Quality Control or Manufacturing lab, • Highschool Diploma/GED is required, BS in STEM degree is a plus, • Ability to lift 50 Lbs. & work across multiple sites, • Familiarity with Lab standards, compressed gas and laboratory utilities, generators, HVAC, IT & access control, • Familiarity or experience working in GxP, a cleanroom and/or a biomedical laboratory environment, • Excellent time and project management skills and proven ability to meet goals and deadlines, • Demonstrated ability to build, repair and maintain equipment, fixtures and furniture, • Demonstrated abilities to learn new skills and fields, creatively solve challenging technical problems, think, • independently, and work collaboratively in diverse multidisciplinary teams, • Entrepreneurial spirit and drive to positively impact global human health Vaxess is building a team of exceptional people to rapidly advance product development. We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you’re interested in joining the Vaxess team, please submit your CV/resume to .

Bio-Rad is seeking a Field Service Engineer based in the Boston. MA area to area to perform repairs, upgrades, and preventive maintenance on our Life Science instruments for customers in hospitals and laboratories. As a Field Service Engineer, you may also be asked to travel on short notice to support other team members within the region. Whether a routine maintenance call or troubleshooting a problem and finding solutions, as our Field Service Engineer, you will play a leading role in supporting the onsite technical needs of Bio-Rad customers. In this highly autonomous role, you will spend the majority of your time at customer sites, with travel up to 5 days a week in your assigned territory as part of a national service team. No day or week will look the same, and your work will have a direct impact on Bio-Rad's success! The environment and culture for this role is fast-paced and you'll be constantly "on the go". It requires the ability to solve complex problems while maintaining strong relationships with our customers. How You'll Make An Impact: • Performing repairs, upgrades, and preventative maintenance on Bio-Rad's instruments, ensuring the quality performance of our instruments for customers who are working to advance the future of healthcare., • Supporting and maintaining the Bio-Rad instruments on which our customers rely on to make scientic breakthroughs helping to advance healthcare research and treatments., • Building and sustaining strong relationships allows you to anticipate and advocate for our customers needs. While the list of qualifications may help an employee to succeed in this position, capable candidates may have a wide range of backgrounds and skills. If you have experience that aligns with the responsibilities of this role, we encourage you to apply! • At least 1 - 3 years of transferable field service experience servicing electro-mechanical/electronic/optical/robotics equipment and an A.S. or B.S. in Electronics, Biomedical Engineering, or Mechanical Engineering (or a related field or military equivalent experience)., • Ability to read, understand and successfully follow medium to highly complex work instructions., • Strong electro-mechanical troubleshooting skills., • Strong computer skills and fundamental knowledge of computer networking., • Strong customer relation and communication skills, both written and oral. Total Rewards Package: At Bio-Rad, we're empowered by our purpose and recognize that our employees are as well. That's why we offer a competitive and comprehensive Total Rewards Program that provides value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Bio-Rad's robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee's work and life cycle. Benefits: We're proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability, paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG's), and more! Compensation: The estimated base salary range for this position is $80,600 to $110,800 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance. Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply. Agency Non-Solicitation:Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes. Fraud Alert: Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake "recruiters" and job scams. ___ for more information on this scam and how to avoid it. #LI-JS1 Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.

Job Description Verve is building a world-class team to commercialize wearable solutions that empower the way people move in the world. Our first product is a lightweight, connected wearable system that can be worn all day, every day by industry associates to improve worker safety, and experience. Verve is growing and launching partnerships with some of the leading companies in the world to augment and protect their workforce and we have the unique potential to change the lives of millions of workers. Verve is dedicated to building a diverse team of individuals who are committed to contributing to an inclusive environment and value respect for all, serving the greater good, and welcoming individuals from a wide range of backgrounds, experiences, and perspectives. Role • Design and execute field data collection campaigns — define sensor configurations, sampling protocols, and labeling procedures to build high-quality training datasets from real warehouse environments, • Design experiments to evaluate model performance, isolate variables, and validate hypotheses across diverse worker populations and facility layouts, • Build and maintain ML pipelines that process multi-modal sensor data (IMU, accelerometer, load cell, video) into actionable classifications and metrics, • Engineer discriminative features from time-series sensor signals and evaluate models using rigorous holdout protocols (e.g., leave-one-subject-out cross-validation), • Develop calibration and normalization strategies that generalize across workers, devices, and deployment conditions without per-user tuning, • Translate raw sensor streams into worker safety and productivity metrics, delivered through reports and dashboards for facility operators, • Work closely with hardware and product teams to understand sensor capabilities and constraints, and feed findings back into product requirements, • BSc in Computer Science, Electrical Engineering, Biomedical Engineering, Robotics, or equivalent, • Understanding of signal processing, time-series analysis, and supervised classification techniques, • Experience with Python data/ML stack: scikit-learn or similar, pandas, NumPy, and at least one framework such as PyTorch, LightGBM, or XGBoost, • 5+ years of experience in applied machine learning, sensor data analysis, or quantitative engineering, • Ability to communicate and analyze test results to a broader team, • Experience in the use of analysis/measurement tools such as statistical hypothesis testing, cross-validation frameworks, and experiment tracking, • Experience designing data collection protocols and managing real-world labeled datasets is a plus, • Experience with wearable sensors, IMU data, or human activity recognition is a plus, • Experience in embedded systems / robotics / sensing / IOT is a plus, • Competitive salary and stock options., • Generous premium coverage for medical and dental insurance., • Unlimited PTO, • The opportunity to make an immediate impact in a fast-growing start-up and industry. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Feeling uneasy that you haven’t ticked every box? That’s okay, we’ve felt that way too. Studies have shown women and minorities are less likely to apply unless they meet all qualifications. We encourage you to break the status quo and apply to roles that would make you excited to come to work every day. Powered by JazzHR 1hYodh8ucy

Job DescriptionAt WHOOP, we're on a mission to unlock human performance and healthspan. WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives. WHOOP is seeking a Senior Machine Learning Engineer to join the Sensor Intelligence Group (SIG), a cross-functional team collaborating across WHOOP Labs, Firmware, and Data Science. This role is central to developing and scaling core physiological signal processing and machine learning systems that power WHOOP’s most foundational health features. You will tackle the complex challenge of extracting reliable insights from noisy sensor data and deploying robust algorithms on constrained edge and cloud environments, ultimately delivering meaningful and personalized metrics to millions of members. This role will contribute to both member-facing and regulated health features, requiring a strong balance of ML rigor, production readiness, and regulatory awareness. Join us in pushing the boundaries of wearable technology and positively impacting people's lives! RESPONSIBILITIES: • Design and train deep-learning (DL) and machine-learning (ML) models to extract valuable insights from large repositories of time-series/biosensor data., • Conduct experiments and perform rigorous testing of the models. Optimize and fine-tune the DL/ML (including Foundation AI models) models for deployment in production systems, considering factors such as computational resources and real-time constraints., • Write clean, efficient, and maintainable code that is production ready., • Stay up to date with the latest advancements in AI/DL research and technologies., • Monitor and ensure the proper functioning of algorithms across our diverse user population, addressing any issues related to data and data quality., • Contribute to ongoing research efforts and explore new features for the Whoop product. Collaborate with engineers from SIG, Data Science and Firmware teams to translate research prototypes into scalable, efficient, and cost-effective ML inference systems., • Prepare comprehensive reports for cross-functional teams., • Own the full lifecycle of ML service(s) from development to deployment. Be ready to partner with data engineers to build and enhance data pipelines, validation tools, and monitoring systems that ensure consistent model performance in production., • Mentor team members in ML engineering best practices., • Develop, validate, and maintain ML algorithms for regulated health features, ensuring compliance with applicable regulatory and quality requirements.QUALIFICATIONS:, • Bachelor's degree in either Computer Science, Electrical engineering, Biomedical engineering, Data Science, Artificial Intelligence, Statistics, or a related field; Master’s or PhD degree preferred., • 5+ years of work experience as a Machine Learning Engineer working on research and development problems (4+ years for those with Master’s degree and 2+ years for those with PhD degree). The requirements may be relaxed for exceptional candidates., • Must have experience working with multiple DL architectures. Experience in training/fine-tuning/deploying Foundation AI models is a Significant Plus., • Solid understanding of ML fundamentals, and particularly DL techniques. At the SIG team, we like to be aware of the mathematics behind the algorithms we use., • Strong experience with time series data, e.g. data pertaining to wearables, physiological signals or any high-frequency sensor data. Familiarity with signal processing concepts and techniques is expected., • Proficiency in Python (scientific stack), ML/DL frameworks and libraries, e.g. PyTorch, TensorFlow., • Demonstrated success in designing and deploying ML inference systems at scale, including real-time and batch architectures is a plus. Experience with cloud computing platforms (e.g. AWS or GCP) is a plus., • Strong communication (both written and oral) and collaboration skills across cross-functional teams., • Strong commitment to embracing and leveraging AI tools in day-to-day tasks, ensuring AI-assisted work aligns with the same high-quality standards as personal contributions., • Demonstrated ability to think innovatively and adapt to changing requirements while consistently producing high-quality reports within tight deadlines.

Under remote supervision, Advanced Sterilization Products' Field Service Engineer I is responsible for. Provides guidance to Customers to include hospital Biomedical engineers along with Field Service. Field Service Engineer/Service Technician (Remote-Boston,MA.

Job Description Location: Somerville, MA Senior Mechanical Engineer – Medical Device Overview: Micro-Leads is a fast-paced early-stage company developing an injectable medical device to treat people with chronic pain with greater efficacy. Our company has extensive expertise in precision implantable medical devices for nerve stimulation and neuromodulation. Role Summary: The primary role of this position is to design and build injectable electrodes for needle delivery and implantable pulse generator housings for next-generation neurostimulator devices. The individual will design electrodes for stimulation and nerve recordings. In addition, the candidate will prototype, build, and conduct mechanical integrity and related tests. The individual will also develop manufacturing processes and work with vendors to manufacture components. The candidate must have significant background in medical device development, implantable electrodes, process development, and verification and validation. The individual should be hands-on and have direct experience working with vendors and design transfer to contract manufacturers. Responsibilities: • Mechanical design of implantable electrodes for neuromodulation, • End-to-end development of assembly and manufacturing processes, • Design of processes for thin substrate laminations and bonding techniques, • Design of microscale assembly techniques, including scaling to manufacturability, • Develop micro-molding, thermoforming, and lamination methods for thin substrates and catheters, • Create 3D assemblies and technical drawings of electrodes and implantable housings using SolidWorks and AutoCAD, • Identify, source, and manage vendors to obtain hardware components on a schedule (e.g. procuring materials, services from machine shops or 3D printing houses, contract manufacturing), • Develop mechanical testing structures and set up accelerated lifetime tests, • Manage engineering personnel as necessary (e.g. junior engineers, technicians, co-ops), • Adhere to Micro-Leads quality management system, understands essential regulatory requirements, and follows standard operating procedures, • B.S. in Mechanical or Biomedical Engineering, M.S. Preferred, • Successful candidates must be able to multi-task and work effectively as part of a small team, • Successful candidates will have excellent benchtop capability including the dexterity to manipulate small structures under a stereomicroscope, • Familiarity with standard tooling for rapid prototyping (e.g. drill presses, saws, welding, soldering, CNC mills), • Experience with precision microscale assembly of silicone electrodes using processes such as injection molding, casting, micro-fluidic molding, etc., • Experience with Class III implantable systems and hermetic manufacturing methods, • Medical Insurance, • Dental Insurance, • Vision Insurance, • Stock Options Company DescriptionMicro-Leads is a fast-paced early-stage company developing an injectable medical device to treat people with chronic pain with greater efficacy. Our company has extensive expertise in precision implantable medical devices for nerve stimulation and neuromodulation.Micro-Leads is a fast-paced early-stage company developing an injectable medical device to treat people with chronic pain with greater efficacy. Our company has extensive expertise in precision implantable medical devices for nerve stimulation and neuromodulation.

Job Description About Vizgen: Vizgen is a rapidly growing company that has commercialized the next generation of single cell spatial genomics tools that enable researchers to gain new insight into the biological systems that underlie human health and disease. The company's groundbreaking MERSCOPE product utilizes MERFISH spatial transcriptomics technology to image RNA molecules with high accuracy and unrivaled detection efficiency at subcellular resolution. MERFISH provides transformative insight into a wide range of tissue-scale basic research and translational medicine in oncology, immunology, neuroscience, infectious disease, developmental biology, and regenerative medicine. For more information, go to The Role: Reporting to Vizgens Field Service Manager and working closely with Vizgen’s Support and Product team members, the Senior Field Service Engineer will provide expert instrument support to customers in the Eastern part of North America for the Vizgen’s MERSCOPE solution. MERSCOPE is an in-situ single cell, spatial omics platform that includes reagents, instrumentation, and analysis software. We are seeking an experienced field support engineer with complex scientific problem-solving skills and the ability to understand and implement solutions to meet customer needs. Responsibilities: • Provide instrument and support coverage for customers in the EMEA territory for installation, preventative maintenance, upgrades, troubleshooting, and repair, • Become subject matter expert on Vizgen’s MERSCOPE technology, including instrumentation, software, network communications, and commercial integration of the platform, • Develop a working knowledge of Vizgen’s consumables with respect to how they impact the performance of the platform, • Work directly with external and internal customers to record complaints, investigate underlying causes, and identify short term or long-term solutions, • Support onboarding of new customers through installation and training on Vizgen’s platform, • Respond promptly to service requests and inquiries to ensure a positive customer relationship, • Document and track customer issues, troubleshooting, and resolutions, • Track, prioritize, and ensure issues are resolved within specified SLA’s, • Work closely with management and other team members to solve technical issues, provide product improvement feedback, and ensure customer satisfaction, • Support coordination, scheduling, and tracking of instruments, service parts, accessories, and tools, • Responsible for editing, writing, and modifying Service and Training manuals, Field Service Bulletins, and SOPs, • Support the selling and management of service contracts, • Train and support field service engineer colleagues as needed, • Travel as needed to support customers on site, • Engineering Bachelor’s Degree or equivalent in biomedical, electrical, mechanical or related field, • 5+ years work experience with at least 3 years as a field service engineer in the life sciences research or diagnostic industry, • Experience with imaging, sequencing, or fluidics instrumentation preferred, • Valid driver’s license, US Passport, and good driving record, • Available to accommodate significant overnight travel, • Ability to lift boxes and equipment up to 60 pounds, • Ability to analyze and manipulate data to understand trends, customer needs and root cause issues, • Proven ability to quickly develop expertise, multi-task, embrace change and innovate in a fast-paced environment., • Excellent communication, interpersonal, and customer interfacing skills, • Highly motivated and successful individual who can build and maintain a positive attitude in a challenging, and fast-paced work environment, • High sense of urgency for resolving customer issues, • Highly organized, disciplined, and efficient in meeting deliverables Vizgen affords equal employment opportunity to all qualified persons regardless of race, color, religious creed, national origin, age, military status, sexual orientation, disability, genetic information, gender identity, gender expression or gender unless based upon a bona fide occupational qualification.

Job Description COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery/success. To learn more about who we are and what drives us, watch our company video here. Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation. At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact. For more information, visit POSITION OVERVIEW: We are seeking a Sr. Fill–Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill–finish suite within a commercial manufacturing facility. The ideal candidate has hands-on expertise in formulation, sterile filtration, aseptic filling, lyophilization, capping, inspection processes, and associated equipment technologies, along with a strong understanding of GMP operations and regulatory expectations. This position partners closely with operations, QA, validation, MSdummyamp;T, engineering, and supply chain to ensure robust, compliant, and continuously improving manufacturing performance. WORK LOCATION: Travel to client sites may be required up to 100% based on project phase and client needs. KEY RESPONSIBILITIES: (This list is not exhaustive and may be adjusted as needed.) • Support design, construction, installation, and qualification of a new commercial fill–finish suite, including cleanrooms, process utilities, and supporting infrastructure., • Contribute to user requirement development, equipment specifications, vendor evaluations, and design reviews., • Support FAT/SAT, commissioning, and qualification activities for fillers, isolators or RABS, lyophilizers, depyrogenation tunnels, autoclaves, CIP/SIP systems, formulation vessels, sterile filtration skids, and inspection machines., • Conduct field walkdowns, verify installation details, and ensure alignment with drawings, Pdummyamp;IDs, and GMP requirements., • Serve as subject matter expert for fill–finish operations including formulation, filtration, filling, lyophilization, capping, and visual inspection., • Partner with Operations and MSdummyamp;T to troubleshoot and resolve technical issues., • Collaborate with Maintenance and Reliability teams to address equipment performance gaps., • Support continuous improvement and process optimization initiatives., • Partner with QA, Validation, and MSdummyamp;T to maintain validated state of aseptic manufacturing processes., • Ensure alignment with regulatory requirements including FDA, EMA, ICH, and Annex 1., • Support continued process verification (CPV), annual product review (APR/PQR), and ongoing process monitoring., • Author, review, and approve GMP documentation, including batch records, SOPs, change controls, CAPAs, deviations, and technical reports., • Generate and maintain engineering lifecycle documentation including impact assessments, URS/FRS documents, FAT/SAT packages, and turnover packages., • Develop and execute commissioning and qualification protocols., • Utilize systems such as building management systems, process control systems, and computerized maintenance management systems. Experience with digital validation platforms such as KNEAT is a plus., • Ensure all work complies with GMP standards, safety expectations, and regulatory guidelines, • Coordinate across engineering, operations, facilities, quality, and validation to ensure successful project execution., • Participate in project planning, scheduling, risk assessments, and milestone tracking. Education • Typically 7 or more years of experience in GMP pharmaceutical or biotech manufacturing., • Strong preference for sterile, aseptic, biologics, or vaccine fill–finish experience., • Experience supporting commercial manufacturing operations in a regulated environment., • Strong understanding of aseptic operations, cleanroom environments, and fill–finish equipment., • Strong documentation and technical writing skills., • Ability to manage multiple priorities in a fast-paced environment., • Strong communication, analytical, and problem-solving skills. Physical Demands: The physical demands described here are representative of the requirements that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reach with hands and arms; talk and listen. The employee is frequently required to walk and sit, as well as to lift and carry objects such as books and files weighing up to 25 pounds. The employee is occasionally required to stand, stoop, or kneel. Specific vision abilities required by this position include close vision and the ability to adjust focus. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job, including moderate noise level, an indoor temperate environment, and light levels that are bright and conducive to minimal eye strain, typical for an office environment. TOTAL REWARDS PROGRAM: We define total rewards as compensation, benefits, remote work/flexibility, development, recognition, and our culture with programs that support each of our reward pillars. This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy our generous flexible paid time off program, company-paid holidays, flexible working hours, and fully remote work options for most positions and the ability to work "almost anywhere." However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India. Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time. LEGAL STATEMENT: Syner-G is proud to be an Equal Employment Opportunity and Affirmative Action employers. All employment decisions, including the recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment (if necessary) are made without regard to the employee's race, color, creed, religion, sex, pregnancy or childbirth, personal appearance, family responsibilities, sexual orientation or preference, gender identity, political affiliation, source of income, place of residence, national or ethnic origin, ancestry, age, marital status, military veteran status, unfavorable discharge from military service, physical or mental disability, or on any other basis prohibited by applicable law. Syner-G is an E-Verify employer.

Job DescriptionCompany Description Brainlab revolutionized digital medical technology with the introduction of software for radiosurgery and surgical navigation. Today, Brainlab is an industry leader in digital surgery, radiotherapy and integrated operating rooms. Serving physicians, medical professionals and patients in 6,000+ hospitals in 121 countries, we’re transforming healthcare to improve the lives of patients everywhere. We employ over 2,000 people in 25 locations worldwide. Close-knit teams made of talented, curious and authentic people are working together toward a common goal. Together we’re dedicated to making an impact. Sound like you? Join and grow with us. Job Description • Manage process and handle complex installations, repairs, and preventive maintenance to ensure the successful utilization of Brainlab products., • Manage and resolve product issues through independent troubleshooting and utilization of engineering expertise., • Identify and communicate service-related trends based on end user experiences and system utilization as a means towards product improvement., • Act as key escalation point for technical regional onsite issues., • Drive continuous technical skill development to improve Customer Support related KPI’s (e.g. equipment uptime, system issue resolution, and customer satisfaction)., • Collaborate and strategize with Product Support team to provide regular content for team calls/meetings (e.g. provide technical knowledge transfer, share best practices, unique system issue cases, etc.)., • Manage communication process with customers, including by providing timely updates before, during, and after installations/upgrades, repairs & other service-related events., • Collaborate and strategize with Regional Support Manager to plan, organize, and implement all assigned service tasks within the region., • Maintain a professional demeanor during all interactions, both internal and external to Brainlab., • Teach end users and staff the process for the proper use of Brainlab equipment., • Manage the process for teaching customers on the services offered by Brainlab (e.g. during warranty, service contract period, and while under Time & Material)., • Keep abreast of developments regarding Brainlab and competitive products and services., • Successfully complete company and product trainings as needed to maintain required certifications., • Complete service documentation in a timely fashion in order to meet regulatory compliance., • Review, evaluate, and update Salesforce documentation for the region., • Manage and implement other special projects as requested by management (e.g. regional product launches)., • Ability to travel 75%+, • Salary range between 65-85k Notwithstanding the foregoing, nothing in this job description alters your at-will employment status. Additional duties may be assigned in the discretion of Brainlab. Qualifications • B.S. in Biomedical Engineering, Electrical Engineering, Mechanical Engineering or IT Technology required., • Must be a self-starter, working without close supervision and be able to successfully manage service activities in assigned territory., • Demonstrated engineering experience with medical devices., • Computer expertise, familiarity, and demonstrated expertise with hardware troubleshooting., • Able to apply critical thinking and perform analysis successfully under challenging conditions in a clinical environment., • Knowledge of medical linear accelerator or microwave RF systems and computer networks preferred., • Robotics and/or electro-mechanical systems service experience preferred., • Proficiency in the use of test equipment and hand tools including oscilloscopes, multi-meters., • Excellent organization and time management skills, and the ability to manage many work streams simultaneously., • Excellent written and oral communication skills., • Professional and confident demeanor., • Works well in a team environment and individually., • Proactively approaches his/her contribution to the organization., • Demonstrates leadership abilities., • High comfort level with software and technology in general., • Work safely in confined areas, including high current/ high voltages modulators (20- 50 kV, 1500A), and use peripheral vision to gauge distances. The confined areas have potential hand/arm ‘traps.’ Depth perception is critical., • Must be able to lift 50 pounds and work on ladders. Additional Information In return for the experiences listed above we will provide a business casual environment, competitive compensation package including medical, dental, life, LTD, STD, and matching 401k benefits and much more. Visit us at: Brainlab, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Brainlab participates in E-Verify. Click here for more information. Click here to also review the EEO Law Poster. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to .

Job DescriptionWe are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and strokes! Are you passionate about driving operational efficiency in clinical operations? Join us as a dynamic Senior Process Engineer to revolutionize our clinical production processes and build out workflows for our team of medical imaging analysts. In this pivotal role, you'll develop key operational metrics, design seamless workflows, and foster team and cross-functional collaboration. You'll work hand-in-hand with our talented 3D CT analysts, as well as our Clinical QA, Software QA, and Product Management teams to propel our clinical operations to new heights as we rapidly scale and commercialize. Be part of our mission to advance cardiac care, at the forefront of transforming clinical operations in a fast-paced, cutting-edge environment! The ideal candidate will have: * Bachelor's degree in Engineering, Biomedical Engineering, or a related field. * 5+ years of experience in process engineering or an operational optimization role with software-as-a-medical-device (SaMD) or medical imaging products. * Lean and/or Six Sigma experience. * Strong eye for optimization and a mindset of continuous improvement. * Excellent problem-solving and analytical skills. * Strong communication and collaboration abilities. * Detail-oriented, with a focus on quality and compliance.Work Location: * This role is on-site, based out of our office in Boston, MA. We operate in a hybrid model with regular in-office collaboration.Salary Range: * The anticipated base salary range for this position at Elucid is $135,00-$165,000. Compensation will be influenced by a wide array of factors including but not limited to internal pay equity, job-related knowledge, skills, education, relevant experience, certifications, and geography as outlined in the job description. At Elucid, we believe the best work happens in a flexible hybrid environment. Boston-area employees are encouraged to work from the office on Mondays and Wednesdays, with the option to come in additional days if they prefer. Fully remote employees outside the Boston area come in as needed. We are an equal opportunity employer and value diversity at Elucid. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability. We understand that self-doubt can sometimes prevent great candidates from applying. If you believe you can make an impact at Elucid, even if you don’t meet every qualification, we encourage you to apply! Powered by JazzHR uJr9yL7KL4

Job DescriptionDescription: Welcome to an inspired career. At Halozyme Hypercon™, a wholly-owned subsidiary of Halozyme Therapeutics, Inc., we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and constantly strive to do more. We embrace transformation and work hard to innovate for the future. We do this together, as One Team – we rise by lifting others up and believe in the power of working together for the collective win. That’s why we need you—to help us make a significant impact by taking on increasingly complex challenges, leaping beyond the status quo, advancing our mission and making our One Team culture thrive. Join us as Engineer I, Process Development, and you’ll be part of a culture that welcomes diversity, thinks differently to solve problems, works collaboratively as one team, and delivers meaningful innovations that impact people’s lives. How you will make an impact Halozyme Hypercon is seeking an curious and enthusiastic Engineer I who will be responsible for operating lab and pilot plant scale unit operations at Halozyme Hypercon. This role reports to a Process Development Supervisor and will support the development of biologically active microparticle suspensions. This individual will join a growing multidisciplinary team of scientists/engineers to contribute to a variety of development activities in a highly collaborative environment. The Engineer I role enables our development of robust scalable manufacturing processes for the Hypercon drug product formulation platform by supporting bench-scale and pilot scale experiments. The Engineer I will set up, tear down and maintain equipment, including the generation or improvement of operating instructions, logs and related batch protocols. They will also be asked to execute experiments under the supervision of a development study leader, including data collection, sampling, and in-process testing. The ideal candidate will have a demonstrated track record of attention to detail and adherence to safety protocols in an operational environment and they will identify opportunities to enhance our operational excellence. Success in this role requires adaptability and the ability to thrive in a fast-paced, team-oriented environment. In this role, you’ll have the opportunity to: • Execute and document process development experiments. Collaborate with development study leader to form experiment plans., • Conduct in process testing to characterize microparticle intermediates and bulk drug product materials such as pH, concentration, density, particle size distribution or other at-line or off-line measurements., • Perform daily lab experiments such as blending, filtration, concentration, etc. for microparticle suspensions, • Document and present experiment results within PD and cross-functionally, • Install, test, qualify, and troubleshoot process equipment. Maintain equipment use and maintenance records. Perform routine preventative maintenance and identify the root cause of equipment malfunctions to minimize downtime, • Collaborate with other Process Development (PD) engineers to optimize manufacturing workflows, • Identify opportunities to improve procedures and make revisions to associated SOPs or development batch records as needed, • Work closely with internal functional groups (analytical, formulation, internal manufacturing) to generate meaningful development data, • B.S. in Chemical, Biomedical, Materials, or Pharmaceutical Engineering, or a related engineering discipline, • A detail-oriented approach to experimentation. Attention to detail and the ability to thoroughly document experimental work, • Strong analytical and critical thinking abilities to enable rapid troubleshooting, • Excellent verbal and written communication skills, • The ability to work independently and efficiently in a fast-paced R&D environment, • Familiarity with standard office software (MS Office). Familiarity with computer programming languages or programable logic controllers (PLCs) is a plus., • Ability to transport large volume containers and move large process equipment, with assistance from others and following applicable EHS guidelines, • Some experience with GMP manufacturing sites preferred, • Full and comprehensive benefit program, including an Employee Stock Purchase Program and 401(k) matching., • Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs and tuition reimbursement. Equal Employment Opportunity Statement Halozyme Hypercon, Inc is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race (including traits historically associated with race, including but not limited to: hair texture and protective hair styles), religion, religious creed (including religious dress and grooming practices), ethnicity, color, national origin, ancestry, age (40 and older), genetic information, disability (mental and physical, including HIV and AIDS), reproductive health decision-making, medical leave or other types of protected leave, domestic violence victim status, political affiliation, medical condition (including cancer/ genetic characteristics and information), sex, gender, gender identity, gender expression, sexual orientation, marital or familial status, citizenship, pregnancy (including perceived pregnancy, childbirth, breastfeeding, or related medical conditions), military or veteran status, or any other status protected by federal, state, or local law. Click here to view the Know Your Rights Poster. Accessibility and Reasonable Accommodations Halozyme Hypercon is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans during our application process. If you need assistance or an accommodation due to a disability, contact Human Resources at . Halozyme Privacy Notice: Applicant Privacy Notice. To all agencies, please, no phone calls or emails to any employee of Halozyme Hypercon about this requisition. All resumes submitted by search firms/employment agencies to any employee at Halozyme Hypercon via email, the internet, or in any form and method will be deemed the sole property of Halozyme Hypercon unless such search firms/employment agencies were engaged by Halozyme Hypercon for this requisition and a valid agreement with Halozyme Hypercon is in place. If a candidate submitted outside of the Halozyme Hypercon agency engagement process is hired, no fee or payment of any kind will be paid. #LI-Onsite

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com About the role Nova Biomedical is building its next generation of automation capabilities across multiple manufacturing sites and is seeking a hands-on Automation Engineer with strong manufacturing support experience, proven mechanical/electrical troubleshooting ability, and a developing skill set in automation integration. This role will support production operations and lead or assist automation equipment projects across our Massachusetts sites, with focus areas that include improving quality, efficiency, capacity, and ergonomics; sustaining and troubleshooting production equipment; and building the foundation for equipment data integration – SCADA/AVEVA Wonderware, OSIsoft PI Historian, and future MES/EBR enablement – in a regulated environment. The ideal candidate brings experience supporting automation equipment and a strong desire to grow further into controls, integration, and digital manufacturing. If you’re passionate about automation engineering and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! What you’ll do Manufacturing Support & Troubleshooting • Own daily technical support for manufacturing equipment across Waltham, Norwood, and Billerica., • Diagnose and resolve issues across mechanical, electrical, pneumatic, and basic control systems., • Coordinate with onsite electricians and technicians to minimize downtime and improve reliability., • Conduct informal system reviews and drive mechanical/controls improvements.Automation & Equipment Projects, • Lead the design, installation, and qualification (IQ/OQ/PQ) of new automation systems, including:, • Robotics/cobots, palletizers, automated dispensing systems, • Vision inspection systems, • Mechanical upgrades and OEM equipment, • Own the creation and execution of URS (User Requirements Specifications) and FRS (Functional Requirements Specifications) for automation projects., • Manage vendor selection, FAT/SAT, and commissioning, ensuring scope, schedule, and quality objectives are met.Controls & Integration (Growing Responsibility Area), • Own and execute connections between equipment and supervisory/data systems, including:, • SCADA / AVEVA Wonderware, • OSIsoft PI / PI Historian, • PLC/HMI platforms (Allen-Bradley, Siemens, etc.), • Future MES / EBR systems, • Resolve PLC/HMI issues (hands-on programming not required; commitment to learn expected)., • Standardize integration templates (tags, alarms, connectivity) as Nova matures its digital architecture.Documentation, Compliance & Validation, • Author and maintain engineering documents: URS, FRS, change controls, test protocols., • Maintain drawings and technical documentation in Nova’s systems (J-Drive, I-Drive, MasterControl)., • Deliver validation packages (IQ/OQ/PQ) in ISO 13485 / FDA QSR environments.Cross-Functional Collaboration, • Partner with Manufacturing Engineering, Safety, Quality, Operations, Facilities, and R&D to deliver results. What we are looking for in you • Advanced mechanical and electrical troubleshooting capabilities., • Strong mastery of PLC systems (Allen-Bradley, Siemens) – required, not optional., • Strong understanding of controls engineering, industrial automation architecture, sensors, instrumentation, motion, and communication protocols., • Experience with SCADA, PI Historian, and equipment data integration – required., • Hands-on experience with robotics/cobots, automated systems, and industrial vision systems., • Proficient in SolidWorks and AutoCAD for equipment and system documentation., • Experienced in writing and maintaining URS, FRS, validation documents (IQ/OQ/PQ), test protocols, and change controls., • Proficient with Microsoft Office, Minitab, and SAP., • Strong analytical and problem-solving abilities with a continuous improvement mindset., • Ability to manage multiple automation projects simultaneously from concept through deployment., • Excellent written and verbal communication skills., • Strong cross-functional collaboration with Manufacturing Engineering, Quality, Operations, Facilities, and R&D., • Hands-on, proactive approach with strong floor presence., • Ability to prioritize and manage work across multiple sites., • Motivated to grow into advanced controls integration, SCADA/MES development, and enterprise-level automation strategy., • Bachelor’s degree in Mechanical, Electrical, Mechatronics, or related engineering field, or equivalent hands-on experience., • Minimum of 8 years of experience in automation and/or manufacturing floor support, preferably within medical device, diagnostics, biotech, or other regulated industries., • Proven experience supporting automation systems, equipment integration, and troubleshooting., • Demonstrated experience delivering URS/FRS, engineering specifications, FAT/SAT, and technical documentation., • Ability to read, create, and interpret mechanical drawings, electrical schematics, PLC/HMI logic flow, and system documentation., • Hands-on experience with:, • PLC programming software (Rockwell Allen-Bradley Studio 5000, Siemens, or equivalent), • HMI platforms, • Vision systems (Cognex, Sherlock, or similar), • Robotics / cobots, • Experience with manufacturing data and automation platforms:, • SCADA / AVEVA Wonderware, • OSIsoft PI / PI Historian, • Equipment connectivity and data integration, • Experience working in regulated environments, including ISO 13485, FDA QSR, GDP, GMP., • Familiarity with CMMS systems (e.g., Mpulse)., • Must live within commuting distance of Waltham, Norwood, and Billerica (no relocation assistance provided)., • Willingness and flexibility to travel regularly across Nova’s Massachusetts sites based on business need., • Ability to stand and walk for extended periods while on the production floor or in the lab (up to 4–6 hours/day)., • Ability to lift, carry, push, or pull items up to 25–30 pounds occasionally (e.g., reagent containers, lab equipment)., • Manual dexterity to handle lab tools, open containers, operate equipment, or input data into systems., • Ability to climb stairs or ladders occasionally to access equipment or elevated workspaces., • Visual acuity and color vision sufficient for reading labels, monitoring equipment displays, and identifying chemical indicators or reactions., • Ability to wear personal protective equipment (PPE) including lab coats, gloves, goggles, face shields, and respiratory protection, as required., • Ability to work in various operations such as chemical processing, PCB, warehouses, analyzer assembly, consumable processing of sensors and strips., • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements (job specific), • Professional development, engagement and events, • Company marketplace for lunch and snacks! (location specific) Schedule/Hours: Monday to Friday, 8:00am – 5:00pm Targeted Salary Range: $120k - $130k per year Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy policy

Job Description Cambridge, MA (In-person) About Us: GT Biosciences is a seed-stage techbio startup building Deliveromics, the first AI-powered, high-throughput, multiplexed in vivo data engine for cracking the design rules of drug delivery. Founded by MIT PhDs and an MIT professor, backed by top-tier investors, we’re creating next-generation, non-viral, cell-type-specific delivery vehicles. We’re a small, fast-moving, science-obsessed team on a mission to make routine in vivo cell reprogramming possible. We’re a small, fast-moving, science-obsessed team on a mission to make routine in vivo cell reprogramming possible. We value transparency and collaboration, and seek teammates who thrive in an open, cooperative environment and want to grow together with the team and the company. Job Description: GT Biosciences is seeking a mission-driven, multidisciplinary LNP Scientist to join our Deliveromics Platform Development team to advance the next generation of non-viral delivery technologies. In this role, you will design and develop novel ionizable lipids, engineer ligand-conjugated lipid nanoparticle formulations, support Deliveromics in vivo screening, and evaluate performance using both in vitro assays and in vivo animal models. You will be responsible for experimental planning and execution, data analysis and interpretation, and the clear communication of results. As one of the earliest scientific hires at an emerging techbio company, you will have the opportunity to shape platform development, collaborate across disciplines, and contribute directly to transformative delivery solutions for genetic medicines. This is a full-time, in-person position based in Cambridge, MA. Responsibilities: * Lead the discovery and development of innovative ligand-LNP delivery technologies, with a focus on improving biological performance, biophysical properties, and in vivo targeting. * Design and develop novel ionizable lipids, ligand-conjugated LNP formulations, and related chemistries for targeted delivery applications. * Develop, optimize, and implement high-throughput assays to evaluate LNP systems, including stability, delivery efficiency, and critical quality attributes, in both in vitro and in vivo models. * Design and execute experiments at the intersection of chemistry, molecular biology, and formulation science, including spatial or sequencing-based readouts when appropriate. * Independently plan, execute, and analyze experiments while also overseeing work performed by supporting scientists. * Stay current with emerging research, technologies, and competitive landscapes across lipid nanoparticles, nucleic acid delivery, targeted therapeutics, automation, and gene editing modalities. * Collaborate closely across chemistry, biology, and automation scientists within the Deliveromics Platform group to troubleshoot challenges and integrate new methods into the screening and development pipeline. * Analyze and interpret experimental data using rigorous quantitative and statistical frameworks; generate high-quality reports and provide actionable insights that inform design decisions and platform direction. * Establish and maintain complete, well-organized documentation, including protocols, SOPs, experimental records, and data summaries to ensure reproducibility and compliance. * Drive process and platform innovation, contributing to technology transfer efforts as workflows mature toward automation, scale, and production readiness. Qualifications: Required: * PhD in Chemistry, Bioengineering, Biomedical Engineering, Biochemistry, Biophysics, or a related field. Exceptional candidates with substantial relevant experience will also be considered, regardless of degree. * Hands-on experience with ionizable lipids, LNP formulation, RNA/LNP nanoparticle preparation, targeted delivery systems, or related technologies, with a strong track record in industry or academia. * Deep expertise in the design, synthesis, purification, and characterization of novel ionizable lipids, lipid conjugates, lipid-like compounds, or related molecular platforms. * Practical experience with lipid biology, LNP formulation development and optimization, and in vitro and/or in vivo assays assessing delivery performance. * Strong problem-solving skills, meticulous attention to detail, and a high level of experimental rigor. * Excellent written and verbal communication skills with the ability to collaborate effectively across diverse scientific and technical teams. * A resourceful, adaptable, and emotionally intelligent team member who thrives in a fast-paced, cross-functional environment. * Ability to work onsite five days per week at our Cambridge, MA location. Nice to have: * Prior experience working with non-human primate models will be a strong plus. * Experiences with nucleic acid chemistry (mRNA, ASO, and siRNA, etc.). * Basic coding skills (e.g., Python, R, or MATLAB). * Hands-on experience troubleshooting liquid-handling platforms or automated lab systems. What we offer * Competitive salary and equity. * Flexible, generous health benefits. * Work with a small, world-class team that values rigorous science and candid collaboration. * Opportunity to work with experts from diverse scientific backgrounds. Equal Opportunity Employer: GT Biosciences is an Equal Opportunity Employer. We celebrate diversity and are committed to fostering an inclusive, supportive environment for all employees. All qualified applicants will be considered without regard to race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, gender identity, or sexual orientation. We don't expect anyone to know everything. We learn together, support each other, and get better every day! If you are ready to make an impact, we would love to hear from you.

Job DescriptionAbout Synolo Therapeutics:Synolo Therapeutics, an early-stage biotechnology company launched by RA Ventures, is pioneering the development of precision-targeted immunotherapies for cancer. Powered by computational protein design and proprietary technologies that yield biological data sets at unprecedented scale and resolution, we are building a pipeline of first-in-class multi-specific biologics with novel functionalities. Synolo was founded by pioneers in the field of protein design and engineering, synthetic biology, DNA sequencing, immunology, and biologics drug discovery and development. About RA Capital:RA Capital Management funds and builds healthcare and life science companies using an evidence-based investment approach informed by TechAtlas, a think tank within RA Capital which analyzes scientific and clinical data from academic literature and industry sources to anticipate how breakthroughs might impact industry stakeholders, physicians, patients, and policymakers. TechAtlas' analyses are captured in a unique collection of competitive landscapes, or ‘maps’, that identify competitive therapeutics, diagnostics, research tools, and/or technological capabilities in a given area. About the Role:Synolo Therapeutics is seeking a collaborative and technically strong Senior Scientist or Principal Scientist to join our Biologics Discovery team. This role is a great fit for an antibody discovery and engineering expert who enjoys hands-on work at the bench, leads through influence and scientific excellence, and thrives in a fast-moving, early-stage biotech environment. In this role, you will play a key part in advancing Synolo’s in-house biologics platform, including the discovery, engineering, and characterization of multispecific antibody therapeutics. You will have meaningful ownership of scientific direction and execution, working closely with cross-functional partners across discovery and development. As a member of a highly engaged team, you will help shape scientific strategy, support strong execution, and contribute to a collaborative, thoughtful, and results-driven culture.Key Responsibilities: • Drive discovery and platform efforts: Lead research activities within the in-house biologics team, achieve project milestones, and advance platform development for biologic discovery and multispecific antibody engineering., • Design and build libraries: Develop antibody libraries using in silico and rational approaches, • Antibody isolation and optimization: Experimentally isolate antibodies with desired properties through discovery workflows and analyze antibody sequences resulting from these workflows. Improve antibody leads through humanization, affinity maturation/optimization, and other engineering strategies to enhance performance and overall quality. Partner with Protein Science and Immunology teams to design, engineer, and refine multi-specific antibody constructs to maximize functionality, • Communicate and collaborate: Present results, recommendations, and next steps to project teams and cross-functional stakeholders to drive alignment, momentum, and program success.Qualifications & Skills:, • Strong knowledge of canonical antibody sequence classes and structural concepts, including experience with alternative formats such as scFvs, VHHs, and multispecific formats., • Hands-on expertise with yeast or phage display methods for antibody engineering, including library construction, panning/sorting, and sequence analysis., • Proficiency with next-generation sequencing (NGS) and its application to antibody discovery and optimization workflows., • Experience with handling significant numbers of sequences and related data, and proficiency in software to process antibody sequence-related data (Geneious Biologics, PipeBio, etc.), • Excellent communication and interpersonal skills, with the ability to build productive working relationships across functions and with external contractors, consultants, and CROs.Education & Experience:, • We recognize that great careers aren’t always linear and welcome applicants from a variety of backgrounds., • PhD, MS, or BS in Biochemistry, Molecular Biology, Biomedical Engineering, Chemical Engineering, or a related field, with a minimum of 12 years (BS), 8 years (MS), or 3 years (PhD) of relevant industry experience., • Title will be commensurate with experience.Preferred Experience:, • Experience interfacing with protein design scientists and ML-related workflows, • Experience with automation and automated workflows for both data-handling and liquid-handling systems

Job DescriptionAt WHOOP, we're on a mission to unlock human performance. WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives. As a Sensor Intelligence Engineer at WHOOP, you will be part of a cross-functional team composed of DSP, Apparel & Accessories, WHOOP Labs, Firmware, and Data Science. You will work on the core, fundamental features at WHOOP. This role is tasked with solving the technically challenging problem of extracting physiological information from noisy sensor data, while enhancing diagnostic tools and control methodologies.RESPONSIBILITIES • Collaborate closely with Data Science and Research teams to enhance user metrics by developing innovative and creative algorithms., • Partner with WHOOP Labs to plan data collections, define acceptance criteria, and assess algorithm readiness for real-world deployment., • Validate wearable technology in clinical settings, analyze biomedical data, and prepare comprehensive reports for cross-functional teams., • Monitor and ensure the proper functioning of algorithms across our diverse user population, addressing issues related to data quality., • Contribute to ongoing research efforts and explore new features to improve the overall performance of our products., • Help establish standards and workflows for data analysis, reporting, and dashboard development., • Participate in software development, debugging, and validation processes to ensure code and results are production-ready., • Utilize expertise in signal processing and time-series analysis to analyze biosensor systems and optimize their performance., • Create and implement mathematical models and machine learning algorithms for processing large-scale data and extracting valuable insights.QUALIFICATIONS:, • Bachelor’s or Master’s degree in applied mathematics, statistics, electrical engineering, biomedical engineering, or a related field., • A minimum of 2 years of industry or research experience in signal processing and/or machine learning., • Ability to work with time-series data; familiarity with core signal processing concepts (filters, spectral analysis/FFT, peak detection, windowing)., • Domain exposure to wearable biosignals and real-world noise and artifacts., • Experience developing back-end tools for data processing and analysis., • Proficiency in C and/or Python programming languages., • Solid grounding in statistical inference (e.g., study design, hypothesis testing, regression analysis, bootstrapping), with the ability to choose appropriate methods and articulate trade-offs., • Familiarity with machine learning libraries such as scikit-learn, TensorFlow, PyTorch, Keras, etc., • Strong communication skills with a track record of concise, visual storytelling and documentation., • Demonstrated ability to think innovatively and adapt to changing requirements while consistently producing high-quality reports within tight deadlines., • Experience with version control systems (e.g., Git), CI/CD pipelines, and cloud computing platforms (e.g., AWS).

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com or aicompanies.com About the role The Staff Embedded Software Engineer will lead the design, development, and optimization of embedded firmware for new product development. In this role, they will drive firmware architecture decisions, oversee development cycles, and collaborate with cross-functional teams to ensure high-performance and reliable firmware solutions. The Staff Firmware Engineer must: be detail-oriented, organized, results-driven, have proven ability to track and complete deadline-driven projects, have outstanding communication/interpersonal skills, be a positive contributor and have a strong commitment to quality. Strong time management, organizational skills, and the ability to multitask are a must. They must be a self-starter whose goal is to get the job done and who is able to balance multiple priorities effectively. They must work closely with the hardware team and mentor others with their knowledge. They will work with outside vendors and pursue new skills, new hardware applications, and new tools to improve firmware/hardware development. If you’re passionate about software engineering and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! What you’ll do • Firmware Development & Architecture: Design, implement, and optimize embedded firmware for microcontrollers, processors, and SoCs., • Technical Leadership: Guide a team of engineers, provide mentorship, and enforce best practices in firmware development., • System Integration: Work closely with hardware, software, and product teams to ensure seamless integration of firmware with system components., • Performance Optimization: Analyze and improve firmware efficiency, reliability, and power consumption., • Code Review & Documentation: Conduct code reviews, enforce coding standards, and create detailed technical documentation., • Troubleshooting & Debugging: Utilize tools like oscilloscopes, logic analyzers, and debuggers to diagnose and resolve firmware issues., • Security & Compliance: Ensure firmware adheres to industry standards, security best practices, and regulatory requirements., • Research & Innovation: Stay updated with industry trends, emerging technologies, and contribute to firmware innovation initiatives., • Experience: 8+ years of firmware development experience, with a strong track record in embedded systems., • Programming Languages: Proficiency in C/C++ and assembly language for embedded development., • Embedded Systems Knowledge: Experience with various operating systems, bare-metal programming, and real-time constraints., • Hardware Familiarity: Understanding of microcontrollers (ARM, PIC, MSP430, etc.), peripheral interfaces (SPI, I2C, UART), ADCs, DACs, and debugging tools. Ability to read schematics and use an oscilloscope, • Beneficial Experience: Experience with chemical sensors and/or floating sensors., • Software Development Tools: Proficiency in version control (Git), build systems, and scripting (Python, Bash)., • Communication & Collaboration: Strong interpersonal skills and ability to work with multidisciplinary teams, • Must be able to use basic office equipment: computer, printer, copier, telephone, etc., • Ability to function in a changing, high-impact position, with deadline and resource constraints, • Ability to travel less than 10% of the time, • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements, • Professional development, engagement and events, • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices Targeted Salary Range: $150,000 - $170,000/year Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy policy

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com or aicompanies.com About the role We are seeking a highly skilled Senior Software Engineer with expertise in developing Windows-based medical device software, The candidate will design, develop and maintain the application with .Net Framework, C#, Winforms and XML, with integrated TCP/IP-based communication protocols. You will have a strong background in building high-performance, scalable and reliable backend systems, with experience in concurrent, multithreaded system design. If you’re passionate about software engineering and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! What you’ll do • Design, develop and maintain robust Windows applications using .Net Framework, C#., • Implement high-performance multithreaded applications., • Develop and maintain TCP/IP socket-based communication systems., • Manage data serialization, configuration, and communication using XML., • Collaborate with cross-functional teams to gather requirements and deliver robust technical solutions., • Participate in architecture design and code reviews., • Troubleshoot and debug complex software issues., • Mentor junior engineers and lead technical initiatives when required., • Experience with multithreading and parallel programming., • Strong Knowledge of TCP/IP protocols, socket programming., • Experience with debugging tools and performance profilers., • Excellent problem-solving, analytical and communication skills., • Bachelor’s or Master’s degree of Computer Science, Engineering, or related field., • The ability to work on a laptop or desktop computer for prolonged periods of time., • The ability to lift at least 15 lb., • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements, • Professional development, engagement and events, • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices Targeted Salary Range: $145,000 - $175,000/year. Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy policy

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com or aicompanies.com About the role We are looking for a Senior AI software engineer to support the Research & Systems Engineering. Facilitating the research, design and deployment of new machine learning/artificial intelligence models, to embed within the current and future products portfolio. Owning the technical responsibility for all Artificial Intelligence (AI) features in the image processing and model training Portfolio. If you’re passionate about software engineering and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! What you’ll do • Design and lead innovative AI projects from beginning to end and provide technical guidance to other team members., • Be able to assist in the breakdown of new AI features into actionable work items, and work with the team to estimate the time and complexity involved them., • Produce coherent and concise technical documentation of AI-based projects, providing summaries and evidence of work completed., • Manage AI model codebases from research to production level., • Communicate with other teams (Systems, Software Development team) to perform team tasks more effectively., • Contribute to the creation and filing of patents to protect intellectual property generated through research efforts, working closely with legal and intellectual property teams as necessary., • Ability to work on multiple projects at one time and deliver to deadlines, • Ability to work in a methodical and organized manner and keep detailed records of all work carried out, • Ability to readily absorb complex bioinformatic concepts., • Excellent problem-solving, analytical and communication skills., • Strong knowledge of biotech industry with focus on cell development practices., • Deep knowledge of convolutional models and latest techniques., • Proficiency in major deep learning frameworks (PyTorch, Keras, Tensorflow), • MSc or higher in CompSci, Mathematics, Physics, AI, Computational Biology or any other relevant quantitative discipline, OR equivalent master’s level work experience delivering AI/ML solutions, • 2+ years of experience applying ML/AI to microscope images or biological problems., • 3-4 years of experience with any of the major deep learning frameworks (PyTorch, Keras, Tensorflow), • Experience with ONNX preferred, • The ability to work on a laptop or desktop computer for prolonged periods of time., • The ability to lift at least 15 lb., • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements, • Professional development, engagement and events, • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices Targeted Salary Range: $145,000 - $170,000/year. Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy policy

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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. 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. Job Description Reports to: Director of East Coast Safety or Engineering Manager along with Chief Engineer, Medical Department: Medical Safety Business Tasks/Responsibilities: • Serve as a customer technical contact., • Interpret medical standards and apply the requirements to products under investigation; including but not limited to IEC/EN/AAMI/CSA 60601-1, ISO 14971, IEC 60601-1-6., • Create and implement test plans; conduct the required tests in accordance with the applicable standard(s), procedures and ensure results are documented., • Ensure that test equipment is calibrated or tested and operates properly., • Interface with and update the lab manager., • Review files and reports prepared by other project engineers; including but not limited to peer reviews., • Conduct preliminary design reviews., • Monitor multiple projects., • Prepare certification reports and related documents (e.g., approval letters, test report forms, etc.)., • Assists department with quoting medical projects., • Assist Sales with closing new work.Qualifications, • Four-year engineering college degree – Biomedical or Electrical discipline preferred or three years progress towards four-year degree, or equivalent work experience., • Prior experience performing certification for medical devices at another test, inspection and certification laboratory preferred but not required., • Support department objectives and company goals., • Be a team player., • Sustain a positive, enthusiastic and professional attitude., • Accommodate requests with a smile and “let me see what I can do” attitude., • Adhere to manager directives., • Maintain a professional appearance and demeanor., • Candidate will be required to sign a non-compete agreement as part of the offer. Additional Information Compensation: • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com or aicompanies.com About the role We are seeking a highly skilled staff Software Engineer to design and develop complex Windows-based software systems.The candidate should have expertise in Visual Studio, .Net Framework C#, and multi-process/inter-process communication, along with strong problem-solving skills. This role combines hands-on architecture and development with technical leadership, mentoring engineers and guiding best practices across the software lifecycle. If you’re passionate about software engineering and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! What you’ll do • Design scalable, maintainable, and high-performance systems using .NET framework and C#., • Architect multi-process/inter-process communication(IPC) solutions (e.g., named pipes, sockets, shared memory, WCF or similar), • Lead hands-on development using Visual Studio and moden .NET development practices., • Review code and architecture to ensure quality, performance, and maintainability., • Collaborate with cross-functional teams to gather requirements and deliver robust technical solutions., • Troubleshoot and resolve complex technical issues across the stack., • Mentor and guide engineers in design patterns, architecture, and problem-solving., • Participate in planning, estimation, and technical decision-making., • Strong Experience with large-scale or mission-critical Windows applications., • Expert-level knowledge of C# and .NET framework., • Extensive experience using Visual Studio for enterprise-scale development., • Solid understanding of multi-process architecture and IPC mechanisms., • Excellent problem-solving, analytical and communication skills., • Bachelor’s or Master’s degree of Computer Science, Engineering, or related field., • The ability to work on a laptop or desktop computer for prolonged periods of time., • The ability to lift at least 15 lb., • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements, • Professional development, engagement and events, • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices Targeted Salary Range: $150,000 - $185,000/year. Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy policy

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com or aicompanies.com About the role Nova Biomedical is seeking a Principal Firmware Engineer to serve as a senior technical authority within our embedded systems Center of Excellence. This role is responsible for defining firmware architecture and technical direction across multiple products and platforms, ensuring scalability, reliability, security, and long-term maintainability. The Principal Firmware Engineer operates at an organization-wide scope, influencing firmware strategy, setting standards, and guiding complex, cross-functional initiatives from concept through production and lifecycle support. This role partners closely with R&D leadership, hardware, systems, quality, manufacturing, and external vendors to align firmware solutions with business and product strategy. The ideal candidate is a recognized technical leader who combines deep embedded expertise with strong systems thinking, judgment, and influence. They are self-starter, results-driven, and capable of balancing near-term delivery with long-term architectural vision. If you’re passionate about firmware engineering and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! What you’ll do • Firmware Development & Architecture: Design, implement, optimize, and own embedded firmware for microcontrollers, processors, and SoCs across multiple products, platforms, and generations., • Technical Leadership: Guide a team of engineers, provide mentorship, and enforce best practices in firmware development. Establish long-term technical roadmaps for embedded firmware, balancing performance, cost, reliability, security, and regulatory needs. Influence technical direction across teams without direct authority through mentorship, design reviews, and technical leadership., • System Integration: Work closely with hardware, software, and product teams to ensure seamless integration of firmware with system components. Partner with quality, regulatory, and manufacturing teams to ensure production readiness and lifecycle robustness., • Performance Optimization: Analyze and improve firmware efficiency, reliability, and power consumption. Ensure firmware architectures meet applicable safety, security, and regulatory requirements., • Code Review & Documentation: Lead and participate in code reviews, enforce coding standards. Ensure high-quality technical documentation, including architecture specifications, interface definitions, and design rationales., • Troubleshooting & Debugging: Utilize tools like oscilloscopes, logic analyzers, and debuggers to diagnose and resolve firmware issues. Lead root-cause analysis for critical field or production issues and define systemic corrective actions., • Security & Compliance: Ensure firmware adheres to industry standards, security best practices, and regulatory requirements., • Research & Innovation: Stay updated with industry trends, emerging technologies, and contribute to firmware innovation initiatives., • Experience: 12+ years of firmware development experience, with a strong track record in embedded systems., • Programming Languages: Proficiency in C/C++ and assembly language for embedded development., • Embedded Systems Knowledge: Experience with various operating systems, bare-metal programming, and real-time constraints., • Hardware Familiarity: Understanding of microcontrollers (ARM, PIC, Renesas, MSP430, etc.), peripheral interfaces (SPI, I2C, UART), ADCs, DACs, and debugging tools. Ability to read schematics and use an oscilloscope., • Beneficial Experience: Experience with interfacing with chemical sensors and/or floating sensors., • Software Development Tools: Proficiency in version control (Git), build systems, and scripting (Python, Bash)., • Communication & Collaboration: Strong interpersonal skills, ability to work with multidisciplinary teams, and influence across teams., • Must be able to use basic office equipment: computer, printer, copier, telephone, etc., • Ability to function in a changing, high-impact position, with deadline and resource constraints, • Ability to travel less than 10% of the time, • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements, • Professional development, engagement and events, • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy policy

ASSOCIATE DIRECTOR, RESEARCH TRAINING & Q A, School of Medicine, Department of Medicine.ASSOCIATE DIRECTOR, RESEARCH TRAINING & Q A, School of Medicine, Department of Medicine.Boston University Medical Campus -->.The salary of the finalist selected for this role will be set based on a variety of fac

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