243 Research Development jobs in the United States

Job Description

Empower Your Future: At MetOx International, we're pioneering the next era of energy security and abundance through breakthrough superconducting technology. As a Research & Development (R&D) Engineering Intern you'll join a dynamic team committed to strengthening the world's energy systems to make them more resilient, efficient, and reliable.

Based at our global headquarters in Houston, TX, the Research & Development (R&D) Engineering Intern who is passionate about research and technology innovation will be provided with hands-on experience in materials science and process development. You'll support key experiments, assist with data analysis, and contribute to projects that are shaping the future of superconducting technology.

Key Responsibilities

Experimental Design & Testing

• Assist in designing, conducting, and analyzing experiments related to superconducting materials and processes.
• Prepare lab equipment, set up tests, and ensure that all experimental protocols are followed accurately.
• Document procedures, observations, and findings, helping to drive insights that guide future research.

Data Collection & Analysis

• Collect and analyze experimental data to evaluate material properties, performance metrics, and production methods.
• Utilize statistical and computational tools to process results, identify trends, and support R&D conclusions.
• Generate reports and presentations summarizing experimental outcomes and proposing potential improvements.

Materials Characterization

• Perform material characterization using various techniques (e.g., microscopy, spectroscopy, X-ray diffraction) to assess quality, structure, and composition.
• Support the development of new methods for analyzing and enhancing the properties of superconducting materials.
• Maintain laboratory logs, ensuring accurate and organized records of all materials and tests performed.

Collaboration & Communication

• Work closely with cross-functional teams, including process engineers, materials scientists, and production teams, to align research efforts with practical applications.
• Participate in team meetings to discuss research progress, share insights, and receive feedback from senior researchers.
• Assist with presentations and technical documentation to communicate findings to broader technical and non-technical audiences.
• Other duties as assigned.

Minimum Qualifications:

• Currently enrolled in a Bachelor's or advanced (PhD) degree program in Materials Science, Chemical Engineering, Physics, Manufacturing Technology, or a related field.

Preferred Qualifications:

• Previous internship or lab experience in R&D, materials science, manufacturing technology, or a related area.
• Familiarity with processing equipment, vacuum technology, analytical instruments and data analysis software.
• Experience with lab or manufacturing environments focused on experimental research.
• Specific knowledge/experience related to the powder rheology/powder flow studies.

Knowledge, Skills, & Abilities:

• Basic understanding of laboratory safety, experimental design, and materials testing methods.
• Proficiency in Microsoft Office Suite, especially Excel, for data analysis and reporting.
• Strong analytical and problem-solving skills.
• Excellent verbal and written communication skills.

Physical Demands: This position requires the ability to do basic laboratory/shop floor work (e.g. operating manual valves and switches, loading and unloading tape samples, etc.). It also requires sitting at a desk and viewing a computer screen for extended periods while working or performing other office tasks. Ability to move around the office, including occasional standing, walking, and bending to retrieve documents, attend meetings, or use office equipment. Some light lifting may be required, up to 20 lbs.

MetOx is proud to offer competitive benefits including:

• Health, dental, and vision available on the first day of employment
• 401(k) match
• Paid parental leave & adoption assistance
• Educational reimbursement
• And more!

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Job Description

Who We Are:

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.

Role Overview:

The Sr. Scientist is responsible for the implementation, development, and validation of analytical test methods in support of process research, and cGMP production with emphasis on development of LC, GC, GC-MS and LC/MS, ELISA, SEC-MALS, CE-SDS, cIEF, etc) methods for small molecules, ADCs, Oligonucleotides and Peptides Major support functions include sample analysis by various analytical techniques including HPLC, GC, LC-MS/MS, GC-MS, ICP-MS, CE, SEC-MALS, CE-SDS, cIEF, NMR, KF, titrations, and instrumental and wet chemical techniques. Other duties may involve analytical method modification, development, and validation. The incumbent may function as the primary .

Job Description

We are looking for a proven R&D leader to drive the development of a highly advanced Class III medical devices through concept, preclinical, and clinical stages to FDA PMA approval. The ideal candidate has deep expertise in design controls, system development, and design architecture, with hands-on experience managing GLP animal studies, clinical testing, and regulatory submissions. This is a high-impact leadership role shaping next-generation life-sustaining technologies.

Position Summary:
The Director of Research & Development will lead the design, development, and advancement of innovative Class III medical devices through all stages of the product lifecycle. This role is responsible for ensuring compliance with FDA regulations and global standards, driving R&D strategy, and managing cross-functional teams to deliver safe, effective, and commercially viable products. The ideal candidate will have deep expertise in design controls, system development, and design architecture, with a proven track record of successfully bringing FDA PMA devices through preclinical and clinical evaluation to approval.

Key Responsibilities:

• Provide strategic leadership and technical oversight for all R&D activities, from concept through commercialization.
• Oversee design controls, system development, design architecture, and product lifecycle management in compliance with FDA QSR, ISO 13485, and applicable standards.
• Lead planning, execution, and reporting of GLP animal studies, preclinical testing, and clinical studies.
• Partner with Regulatory Affairs and Clinical teams to support FDA PMA submissions and interactions with regulatory agencies.
• Direct cross-functional project management efforts, ensuring projects are delivered on time, within budget, and to specification.
• Guide system-level design reviews, risk assessments, and design verification/validation activities.
• Develop and mentor high-performing engineering and scientific teams, fostering innovation and technical excellence.
• Collaborate with internal and external stakeholders, including physicians, investigators, CROs, and key opinion leaders.
• Monitor and evaluate emerging technologies, competitive products, and industry trends to inform R&D strategy.

Qualifications:

• Bachelor’s or Master’s degree in Engineering, Biomedical Engineering, or related technical discipline (PhD preferred).
• Minimum 10+ years of progressive R&D experience in medical devices, with at least 5 years in a leadership role.
• Proven track record leading development of FDA PMA devices, from concept through clinical evaluation and approval.
• Strong knowledge of FDA design controls, 21 CFR Part 820, ISO 13485, and risk management standards (ISO 14971).
• Direct experience managing GLP animal studies, preclinical testing, and clinical trials.
• Demonstrated ability to manage complex system development and design architecture processes.
• Skilled in project management, resource planning, and cross-functional leadership.
• Excellent communication, collaboration, and problem-solving skills.

Preferred Qualifications:

• Experience with implantable or life-sustaining devices.
• Strong network with clinical and research partners.
• Familiarity with international regulatory submissions (CE Mark, MDR, etc.).

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Job Description

Hygiena provides rapid microbiology diagnostic tests and solutions for mission-critical, time-sensitive processes around the world. Hygiena’s proprietary diagnostic technologies enable customers to; prevent illness and save lives, comply with regulations, protect products and brands, run businesses more effectively. Solutions are sold in a wide range of industries globally, but the core focus is food safety. Headquartered in Camarillo, California and with offices around the world, we are actively looking for talented individuals to help grow the business!

At Hygiena we believe:

• In providing the highest quality products & service
• Being a leader in innovation
• Having a compelling desire to improve and win in the marketplace
• In contributing positively not only in the workplace, but in our community and environment!

With rapid growth comes opportunity. We are looking for a Director, Research & Development to join our team in Camarillo, CA.

The Director, Research & Development (R&D) Microbiology is responsible for managing and leading a team of R&D Scientists who are responsible for creating new products and improving existing products. Increase sales revenue to expand the diversification of Hygiena technology and disseminate the Hygiena brand through advances in R&D.

Responsibilities:

• Manages the R&D team to ensure project goals are delivered in an efficient and timely manner, while ensuring adherence to Design Control Processes and Principles. Assigns projects and SMART goals as directed by the Executive team, aligning projects with marketing requirements. Coordinates program status with Project Management and communicates effectively with senior management teams.
• Develops microbial or biochemistry detection technologies and assays to meet market requirement, maintains brand leadership and improves competitiveness.
• Develops strategies for new product development, organic growth of existing products and utilization of relevant, complimentary technologies.
• Assesses competitor products and new technologies, developing appropriate responses to capitalize on the challenges and opportunities involved.
• Acts as lead thinkers for ongoing strategies for Hygiena, continuing efforts to increase and expand the product portfolio.
• Coordinates with R&D Managers to ensure the R&D teams run effectively. Executes and conducts annual performance reviews in addition to congoing feedback and discussions.
• Performs technical support activities by providing technical advice to manufacturing, quality control, sales, customers and internal technical support teams
• Oversee and lead the department's annual budget and quarterly forecast. This includes identifying and recommending areas for improvement and opportunities. Additionally, collaborate with management teams to prioritize and eliminate expenses to achieve financial objectives and promote financial discipline.
• Ensures compliance with and/or follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seeks guidance as necessary.
• Actively supports and participates in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Safety Manual and Injury Illness Prevention Program (IIPP).
• Carries out all responsibilities in an honest, ethical and professional manner.
• Must be able to fulfill essential job function in a consistent state of alertness and safe manner.
• Handles various other duties as delegated by the Chief Scientific Officer.

Qualifications:

• Master’s Degree in a Microbiological discipline with greater than fifteen (15) years’, or a PhD with greater than ten (10) years’ working experience in a professional laboratory at management and strategic levels.
• Must have practical and working knowledge of the following:
• Microbiology, Biochemistry, Bioluminescence.
• Management of R&D teams, ideally in a different location.
• Current developments in the market.
• Manufacturing expertise.
• Working knowledge of statistical methodologies.
• Deep and current understanding of microbiological methods.
• Project management skills and experience
• Advanced knowledge of Microsoft Office (Outlook, Word, Excel, PowerPoint) and Adobe Acrobat required.
• Good understanding of our customers and market, and industry associations and networks.
• Management experience of several teams and external associations
• Working knowledge of Design Control Processes
• Working knowledge of current markets for Hygiena

Salary Range (applicable to California):

$190,000.00 - $205,000.00 base salary DOE

Supervisory Responsibilities:

In accordance with applicable policies/procedures and Federal/State laws, may perform the following supervisory responsibilities: Interviewing, hiring, orienting and training employees; planning, assigning, and directing work; coaching and appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; enforcing all safety rules and ensuring safe work procedures.

Skills/Abilities:

• Excellent verbal and written communication,
• Must be able to use discretion and independent judgement.
• Must be able to work in a team environment.
• Must be able to pay close attention to details.
• Must be able to adapt and flex to a changing environment.
• Must be able to lift/carry 20 pounds.
• Microbiology expertise: aseptic technique, media prep, plating, dilutions, microbial classification and physiology
• Show good self and situational awareness
• Ability to take control during presentations to senior management
• Leadership skills, can mentor and be an arbiter for team members

Working Conditions:

• Is required to work normal office hours (with some flexibility as per the below) Monday through Friday in the Office
• May occasionally work early morning/evenings/weekends to accommodate urgent customer requests in different time zones
• Will be required to travel to represent Hygiena approximately 20% domestic and internal travel including customer visits, regional offices, and industry events.
• May occasionally work evenings and/or weekends.

Why you’ll want to join our team:

Teamwork as a core value.

At Hygiena, our emphasis on teamwork and cross-functional communication enables us to build stronger bonds within our business.

Be a part of something big .

Hygiena plays a critical role in helping to prevent global health crisis such as foodborne illness, healthcare-associated infections, and other outbreaks.

Giving back to our communities .

Hygiena believes in giving back by supporting local organizations committed to improving the lives of children and youth in our communities.

Benefits and Perks:

• 15 days of PTO & 9 paid company holidays
• Medical with HSA employer contribution, Dental, Vision available 1st of the month after start date
• Company paid Life Insurance, Short* and Long-Term Disability and an Employee Assistance Program
• 401(k) with Safe Harbor and Profit-Sharing employer contributions
• Tuition Reimbursement program
• Charitable Contribution matching
• Employee Referral bonus opportunities

*State paid short-term disability for California based employees

We are an equal opportunity employer and value diversity. All employment is decided on the basis of qualifications, merit and business need. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Hygiena participates in E-Verify.

Job Description

Research and Development Engineer

Job Type : Full-time, Exempt

Position(s): 1

Reporting to : Head Research and Development.

Location : Pocahontas, AR.

About Us

At Tate we are passionate about everything we do. Tate has been recognized worldwide as an industry leader in the development and manufacture of data center infrastructure solutions, for over 60 years. We have expanded our manufacturing footprint across the US, Canada, Europe, Australia and are excited to have opened a new 287,000 sq. ft. manufacturing site in St. Paul, Virginia, and an additional 40,000 sq ft of manufacturing at our site in Belgium in Q1 2024 alone.

Our experienced team is expanding, and we are excited about our fresh, dynamic, and inclusive team of experts working collaboratively on projects, as we continue to stay ahead of the data center revolution. We continue to invest heavily in the best available manufacturing tools and equipment needed to adhere to Tate’s world class standards and our business remains committed to developing lower carbon, sustainable solutions, in keeping with our 10-year Planet Passionate sustainability strategy. We are excited to potentially welcome you as part of our team. Together, let's shape the future of data center infrastructure with innovation, excellence, and a passion for sustainable growth.

At Tate, you can expect the stability and growth of a long-established multinational coupled with the speed and dynamism of a fast-paced growing company. The perfect balance!

About the Role

As an R&D (Research & Development) Engineer at Tate, you will be a key contributor to our organization’s future, collaborating with diverse teams to drive cutting-edge research and development initiatives. In this role, you will assist in the development and testing of innovative solutions, while playing a crucial part in creating mockups and performing various production tasks, including packaging. Your hands-on work will involve prototype construction, assembly, and evaluation, along with supporting the continuous improvement of our production processes. This newly created role within our R&D team offers a unique opportunity for ambitious individuals to make a tangible impact and pave the way for a promising future at Tate.

What You’ll Do

• Design, develop, and test new products and technologies.
• Collaborate with cross-functional teams to brainstorm ideas and solve technical challenges.
• Conduct research and analyze data to identify emerging trends and opportunities for innovation.
• Assist in implementing experimental protocols and procedures for R&D projects.
• Support the documentation of project progress, including writing reports and maintaining records.
• Participate in prototype construction, assembly, and evaluation to validate design concepts.
• Engage in creating mockups and other hands-on production tasks to bring designs to life.
• Assist in the optimization of existing production processes and workflows to enhance efficiency and quality.
• Stay updated on industry trends, best practices, and emerging technologies to drive continuous improvement in R&D and production practices.

What You’ll Bring

• Bachelor’s degree in engineering
• A minimum of 5 years of relevant experience
• Strong experience within production, assembly, and hands on technical work
• Strong academic background with coursework in mechanics, materials science, and engineering design.
• Proficiency in CAD (Computer Aided Design) software (e.g., SolidWorks, AutoCAD) for design and drafting purposes.
• Experience with simulation and analysis tools such as Finite Element Analysis (FEA) or Computational Fluid Dynamics (CFD) is advantageous.
• Excellent problem-solving skills, attention to detail, and the ability to work effectively both independently and as part of a team.

Employee Benefits

• Career Scope and Advancement: As we continue to grow (USA Canada, Ireland, and Australia) new positions and opportunities are available, offering some accelerated careers (locally and globally) for the right person.
• Corporate Social Responsibility: Through Planet Passionate we are determined to reduce our manufacturing carbon (CO2e) emissions to as close to zero as technically possible, together with halving carbon intensity in our primary supply chain. We are very involved in our community, and you will have ample opportunities to support us in creating a better world.
• Skills Development: With the fast-paced nature of our business and high degree of collaboration, your new role is diverse and multifaceted – making you a more versatile employee with a broadened skill set.
• Recognition and visibility: As we expand, there is a greater chance for our senior leaders to notice your wonderful contributions and efforts. We love to celebrate success at Tate.
• Entrepreneurial Spirit: You will have the chance to take ownership of projects, make decisions that shape the company's direction, and innovate without bureaucracy.
• Mentorship and development: At Tate we don’t believe in hierarchy, we work together as one team for one common goal. You will have access and exposure to our senior leaders and experts for learning in your role, and additionally mentorship for the future.
• Culture : We have a great team culture, highly collaborative, supportive, and social. Together we innovate, collaborate, and work together to provide excellence.

Employee Benefits

• Career Scope and Advancement: As we grow, new positions and career opportunities arise, offering accelerated paths for the right candidates, locally and globally.
• World of Wellness Philosophy: We empower you to take charge of your health and well-being. You’ll have access to a wide range of medical, dental, and vision benefits, along with personalized guidance from a “Health Advocate.” We also offer other supplemental options, including 401k, legal, disability, and theft insurance, to ensure your financial wellness.
• Corporate Social Responsibility: Through Planet Passionate we are determined to reduce our manufacturing carbon (CO2e) emissions to as close to zero as technically possible, together with halving carbon intensity in our primary supply chain. We are very involved in our community, and you will have ample opportunities to support us in creating a better world.
• Skills Development: Given the dynamic pace of our business and a strong collaborative environment, your new role will be diverse and multifaceted – allowing you to be more versatile and develop a broader skill set.
• Mentorship and development: At Tate, we don’t believe in hierarchy, we work together as one team for one common goal. You will have access and exposure to our senior leaders and experts for learning in your role, and additionally mentorship for the future.
• Culture: We have a great team culture, highly collaborative, supportive, and social. Together we innovate, collaborate, take ownership, and strive for excellence.

Tate is an equal opportunity employer. We welcome applicants from all backgrounds and do not discriminate based on race, religion, gender, sexual orientation, age, disability, or any other protected status. Come aboard as we champion diversity and inclusivity in the workplace!

Stay connected with us on LinkedIn for insights into life at Tate. Join us in our mission to make a difference through exceptional solutions.

Job Description

Overview

We are seeking an innovative and experienced R&D Lead – Electrical Engineering to drive research and development initiatives at AUTEC Car Wash Systems. This role combines technical expertise in electrical and control systems with leadership in new product development, testing, and innovation. The ideal candidate will guide R&D projects from concept through implementation, ensuring designs are reliable, cost-effective, and aligned with AUTEC’s commitment to quality and innovation.

Responsibilities

• Lead electrical engineering efforts within the R&D team, driving the design, development, and testing of next-generation car wash systems.
• Manage and prioritize multiple R&D projects, balancing innovation with practical manufacturability.
• Design, program, and validate control systems using PLCs, relays, timers, VFDs, and other industrial automation components.
• Oversee prototype builds, experimental testing, and field trials, ensuring rigorous evaluation of new designs.
• Collaborate with cross-functional teams (Mechanical Engineering, Software, Operations, Service) to integrate new technologies into AUTEC’s product line.
• Create and maintain accurate technical documentation, including schematics, BOMs, test protocols, and reports.
• Research and implement emerging technologies, materials, and processes to improve system performance, efficiency, and safety.
• Provide technical mentorship to junior engineers and contribute to team training and development.
• Ensure R&D projects comply with applicable codes and standards (NEC, UL 508A, OSHA, NFPA).
• Present findings, progress updates, and recommendations to leadership and stakeholder

Qualifications

• Education & Experience: Bachelor’s or Master’s degree in Electrical, Controls, or Automation Engineering, with 5+ years of relevant engineering experience and 2+ years in a leadership or project lead role.
• Technical Skills: Advanced proficiency in PLC programming (Siemens, Mitsubishi, GE), ladder logic, HMI development, and industrial automation systems.
• Industry Knowledge: Experience with AutoCAD Electrical or SOLIDWORKS Electrical; working knowledge of VFDs, servo systems, pneumatics, hydraulics, and wire harness design. Familiarity with SAP preferred.
• Leadership Skills: Demonstrated ability to lead cross-functional teams, manage R&D projects, and mentor engineering staff.
• Other Skills: Strong analytical and problem-solving abilities, excellent communication skills, and the ability to balance innovative ideas with practical execution.

• Regularly required to use hands to handle or feel objects, tools, or controls.
• Frequently required to stand, sit, reach with arms, talk, and hear.
• Occasionally required to walk, climb, balance, stoop, kneel, crouch, or crawl.
• Must be able to regularly lift and/or move up to 10 lbs, frequently up to 25 lbs, and occasionally up to 50 lbs.
• Specific vision abilities include close vision, depth perception, and the ability to adjust focus.
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this role.

Job Description

Who We Are:

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.

Role Overview:

The Scientist I - Process Research & Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget.

Core Responsibilities:

• Delivers experimental output with a high scientific integrity, both on time and target, and of high quality with guidance.
• Exhibits safety awareness, safely conducts lab and other operations and hold themselves accountable for safe behavior in the work environment.
• Maintains technical equipment and services.
• Acts on feedback and show continuous commitment to learning and development.
• Lead technical and operational areas and support troubleshooting for complex scientific issues under minimal guidance.
• Expertly shares knowledge, skills and experience, communicating internally and externally. May lead focused projects as key .
• Legitimate LinkedIn communications will only come from active Veranova employees.
• Veranova will never ask candidates for sensitive personal information during the application process (e.g.,

Job Description

About GrapheneDx: GrapheneDx is a new diagnostics technology company with a mission to transform consumer diagnostics. Our employees gain experience in a multidisciplinary, fast-paced start-up and have ample opportunities to acquire new skills, engage with emerging technologies, and collaborate closely with an accomplished team, all within in a supportive and energetic environment.

GrapheneDx offers a competitive compensation package including base salary, performance bonuses, paid time off, health and dental benefits, and excellent growth opportunities.

GrapheneDx is seeking a Research Scientist who will apply their expertise to advance our R&D efforts in biosensor development and communicate valuable insights to a highly collaborative and dynamic team.

Summary: The Research Scientist in Assay Development will design and execute experiments to functionalize sensors with nucleic acid or antibody probes for biomarker detection, contributing to the development of a groundbreaking, point-of-care diagnostic platform. Collaborating closely with a senior scientist and a cross-functional team of materials scientists, electronics engineers, and data scientists, this role drives forward a disruptive diagnostic technology poised to redefine the field.

Key Duties and Responsibilities:

• Drive the development of a novel GFET-based point-of-care diagnostic platform.
• Design, execute, and optimize experiments for biomarker detection, including feasibility, pilot, and process optimization studies.
• Perform data analysis, critically interpret results, and prepare reports and presentations tailored to the needs and expertise of internal and external stakeholders.
• Collaborate with a cross-functional team of scientists and engineers to design experiments aligned with R&D objectives, ensuring sensor technology integration into scalable diagnostic solutions.
• Document, refine, and optimize protocols, creating actionable plans to improve processes and advance R&D milestones
• Identify and troubleshoot technical challenges, contributing to regulatory documentation, and ensure protocol compliance where relevant.

Essential Experience:

• Ph.D. in Biochemistry, Biology, Chemistry, Electrochemistry, Biophysics, or a related discipline, or a Master’s degree with 1-5 years of relevant academic or industry experience.
• Proven experience in creating and developing biosensor immunoassays and/or nucleic acid detection assays through probe hybridization.
• Strong problem-solving skills, with the ability to identify challenges and propose alternative approaches.
• Excellent organizational and analytical skills, including the ability to summarize and translate data into actionable plans.
• Effective oral and written communication skills to convey technical information to both supervisors and team members.

Desirable Experience:

• Experience with non-optical-, electrical-, or electrochemical-based sensors, especially graphene-based or carbon nanotube-based sensing platforms.
• Experience functionalizing GFETs with biological probes, such as nucleic acids or antibodies, to enable biomarker detection.
• Experience defining and improving biosensor performance metrics, such as sensitivity, specificity, limit of detection (LOD), and other industry-standard used to quantify biosensor efficacy and reliability.
• Proficiency in coding or data visualization using Python, Origin, and/or Minitab for data analysis and visualization.
• Working knowledge of statistical analysis and design of experiments.
• Ability to coordinate effectively across multiple functional areas.
• Highly motivated and adaptable, with the flexibility to thrive in a dynamic and interdependent environment.

POSITION SUMMARY:

We are seeking a hands-on, innovative Additive Research & Development Engineer to join our elite Castheon team. This role is ideal for someone passionate about pushing the boundaries of metal additive manufacturing and material science. You will develop and optimize AM process parameters, support material characterization, and lead R&D initiatives to unlock next-generation applications in critical industries.

If you're ready to transform the future of manufacturing and thrive in a fast-paced, high-impact environment, apply now and become a vital part of the ADDMAN innovation engine.

LOCATION:

Onsite at our facility locally known as Castheon: 2201 Corporate Center Dr, Thousand Oaks, CA 91320

ESSENTIAL JOB FUNCTIONS:

• Develop and refine print parameters for various metals (e.g., Ti-64, Inconel 718, C103) across multiple additive platforms (LPBF, DMLS).
• Lead experimental builds, analyze output, and implement feedback loops to optimize print quality and mechanical performance.
• Design and execute material qualification plans, including tensile, fatigue, and creep testing in collaboration with internal and external labs.
• Apply metallurgical analysis (SEM, EDS, XRD, microscopy) to evaluate build integrity, powder characteristics, and defect mitigation strategies.
• Partner with manufacturing and quality teams to transition R&D outcomes into production workflows.
• Conduct root cause analysis and corrective action for anomalies in printed components.
• Collaborate on DoD and aerospace projects, contributing technical documentation and test reports for customer and regulatory approval.
• Stay up-to-date on the latest developments in AM standards, equipment, and materials and integrate them into our process development roadmap.

ITAR REQUIREMENTS:

• This position is subject to the International Traffic in Arms Regulations (ITAR) which requires U.S. person citizenship status.

SKILL REQUIREMENTS:

• Commitment to a safety culture where safety is the first consideration before starting any task.
• Excellent verbal & written communication skills, including public speaking and meeting facilitation.
• An all-embracing attitude capable to internal motivation.
• Strong organizational skills and attention to detail.
• Ability to work in a team-oriented environment that is fast paced and demanding.
• Ability to perform duties with the highest level of integrity and ethics.
• Well-organized with a systematic approach to responsibilities.
• Ability to develop and maintain effective working relationships.
• Advanced analytical and problem-solving skills.
• Proven ability to assess situations and develop plans to achieve resolution.
• Advanced knowledge of Microsoft Office Suite. Skilled in Excel (formulas, pivot, data maintenance)

QUALIFICATIONS:

• Bachelor’s or Master’s degree in Materials Science, Metallurgy, Mechanical Engineering, or a related field.
• 3+ years of experience in metal additive manufacturing, ideally in an R&D or advanced engineering setting.
• Deep knowledge of additive manufacturing principles, especially LPBF/DMLS systems.
• Experience with material characterization techniques and mechanical property testing.
• Familiarity with AM simulation tools, CAD software (SolidWorks preferred), and data analysis (Python, MATLAB, or Minitab a plus).
• Hands-on experience with parameter development and laser strategy tuning is preferred.
• Background in defense, aerospace, or regulated industries with complex qualification path is preferred.
• Exposure to microstructure evolution, post-processing (HIP, heat treat), and failure analysis is preferred.
• Understanding of AM standards (AMS7000 series, ASTM F42, etc.) is preferred.

BENEFITS START ON DAY 1:

• Medical, Dental, and Vision plans
• Life Insurance and long-term disability insurance
• Flexible Spending