Research and development technician jobs in Prunedale, CA - 226 jobs

Medical Device R&D Technician Pay $35-38 6 month+ assignment Onsite in Campbell, CA Assemble fluidic tube sets, mechanical gear, and catheter-based devices in a clean room environment through adhesive bonding and cure, mechatronic assembly and electrical/mechanical testing. Demonstrated history of working on complex mechanical and electrical systems. • HS diploma and a minimum of 8 years related experience; AA degree and a minimum of 5 years experience preferred. • Strong understanding of assembly and calibration methods. • A proven ability to work well in a team environment • Must be capable of working independently and in a team while being flexible and self-motivated. • Previous experience assembling Medical Devices in an FDA-regulated environment is preferred. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Assemble complex mechanical systems that encompass hundreds of unique parts. Your expertise with precision tools will ensure the accurate placement of linear guides, rotary bearings, actuators, motors, and drive systems. • Collaborate closely with engineers to develop work instructions, maintain inventory for development builds, and ensure a clean and organized build environment. • Maintain and calibrate tools, replenish stock fasteners, and ensure organization in the development and build areas. • Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy. • Assure that you and functional subordinates (if applicable) are trained on all applicable procedures and processes according to Good Manufacturing Practices, and applicable FDA and Regulatory requirements. • Actively promote and support the company's Management Review process. • Inform responsible personnel of concerns involving product quality. Benefits (employee contribution): Health insurance Health savings account Dental insurance Vision insurance Flexible spending accounts Life insurance Retirement plan All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

It's Time to Join Stryker! Why Join Us? At Stryker Endoscopy, we're not just testing products - we're redefining how they perform in the real world. We're looking for analytical problem solvers who go beyond validation, characterizing designs, identifying root causes, and recommending comprehensive improvements to prevent future issues. You'll think like a user, design and test with purpose, and collaborate across disciplines to develop products that improve patient outcomes and empower caregivers worldwide. What You Will Do As a Senior R&D Test Engineer, Electrical, you'll join a close-knit, cross-functional R&D team that experiments with prototypes, validates designs, and ensures the safety, performance, and reliability of next-generation surgical imaging products. You'll act as both a hands‑on engineer and a key technical partner, helping transform concepts into real‑world solutions. You will: Lead and execute test plans for electrical subsystems and integrated products from prototype through verification. Develop and document test methods, protocols, and reports in compliance with design control and quality system requirements. Build and debug test fixtures, leveraging coding or automation tools (Python, LabVIEW, C/C++). Provide early design feedback to cross‑functional teams and collaborate closely with design engineers to resolve technical challenges. Use standard lab equipment (oscilloscopes, signal generators, power supplies, protocol analyzers) to perform detailed electrical characterization and reliability testing. Guide or mentor others (interns, specialists, or peers) while independently managing your test activities and timelines. Contribute to system‑level test development that spans hardware, firmware, and software integration. Partner with teams across sites and occasionally travel to support cross‑location initiatives. What You Will Need Required: Bachelor's degree in Electrical Engineering, Computer Science, Biomedical Engineering or a related discipline. 2+ years of related engineering experience Preferred: Experience in medical device or other regulated industries Hands‑on test engineering experience with analog and digital circuitry Proficiency with electrical lab instruments and automated test scripting (Python, C/C++, or LabVIEW) Experience developing, executing, and documenting component‑or system‑level testing Familiarity with defect tracking and documentation tools (e.g., Jira) Understanding of design controls, reliability testing, and quality systems Strong communication skills, initiative, and the ability to work both independently and collaboratively $100,400- $160,800 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. #J-18808-Ljbffr

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply. Job Description: High-Throughput Screening Research Associate II, III (Biodesigner II, III) Responsibilities: Perform massively parallel reporter assays and high-throughput screens across diverse cellular contexts using cellular and molecular readouts. Develop and execute molecular biology workflows such as vector design and cloning, DNA/RNA extraction, RT-PCR, qPCR, and next-generation sequencing. Support cell culture activities and experiments in multiple cell lines, at small and large scales. Design and execute cell-based assays (AAV/lentiviral transduction, transfection, flow cytometry, immunostaining, and other plate reader assays). Engineer and characterize cell-based systems using synthetic biology tools and techniques. Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to optimize screening throughput, sensitivity, and specificity. Proactively troubleshoot technical issues and recommend potential corrective actions based on personal observations and literature searches. Prepare summaries of data and present internally to colleagues and management. Draft SOPs, follow protocols, diligently document experimental data in lab notebooks, and organize and maintain electronic work records. Author scientific reports and data summaries. Collaborate with cross-functional teams to meet project goals, bridging early discovery with high-throughput screens to nominate and optimize candidates for further characterization. Qualifications: Bachelor's or Master's degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. At least 2 years of industry wet lab experience. Mammalian cell culture experience (culturing, transfecting and transducing cells, and DNA/RNA purification from cells). Molecular biology expertise (vector design and cloning, qPCR, primer and probe design, DNA/RNA extraction workflows) Critical thinker with excellent communication skills who thrives in a multidisciplinary, fast-paced team environment. Strong written and verbal communication skills. Preference will be given to those who display: High throughput screening assay development in an industry setting. High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. First-principles thinking, and an ability to refine one's intuition based on additional data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. High EQ with team-oriented thinking. Experience with pooled, high-throughput screens using next-generation sequencing-based readouts, and/or preparing screening plasmid libraries from synthesized oligo arrays. Experience with CRISPR-Cas systems and/or gene editing and delivery technologies. Experience preparing next-generation sequencing libraries (Illumina, PacBio, and/or Nanopore platforms). If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

We are a group of people united by a strong purpose. We want you to get to know us, and Giuseppe, our very own artificial intelligence. We love good food, but above all, we love the planet, and that's why, to protect it, we reinvent the food industry, one delicious bite at a time, elevating what we eat, through our technology and based on plants. Our recipe has three mega-important components: science, technology, and of course, disruptive talents who work daily to create a better future. At NotCo we are not and do not seek to be the perfect company, but rather the right one. We are here to produce changes, and that is why we dare, fail, and sometimes achieve incredible successes. We are currently looking for a Product Development Scientist for our NotCo B2B Research & Development located in San Francisco, California, requiring an active on-site presence. This position will report to our R&D Sr. Team Lead and the incumbent will work cross-functionally to ensure R&D activities are successfully deployed locally. Responsible for the: Independently conducts day-to-day product development activities as directed by the manager across multiple projects. This includes supporting activities related to the full product lifecycle process (from product concept to successful commercial launch as needed)and supporting process development, scale-up and technology transfer Supports the design and execution of bench-top tests, pilot-plant trials and full-scale formulations to deliver high-quality food products that meet and exceed the sensory, cost, and other performance targets Proactively proposes and uses sensory and analytical analysis to guide and validate the development process Maintains detailed documentation, experiment tracking and outcomes, and documents finished goods and ingredient specifications Provides feedback to project lead regarding relevant technical and process information Communicates proactively and effectively with cross-functional teams, clearly articulating perspectives and trade-offs related to new product development goals Utilizes NotCo's proprietary AI technology to develop and improve food products Supports formula validation activities as well as process development, scale-up and technology transfer Engages in client communications and workshops, bringing technical Maintains detailed documentation across all R&D activities in a timely manner Qualifications / Requirements: Bachelor's degree in Food Engineering, Food Science, Engineering in Biotechnology or a similar discipline. 2 + years of Food R&D experience is desired, preferably across both food and beverage categories. Be agile, adaptable, and thrive in a dynamic and changing culture; works relentlessly to overachieve, anticipate obstacles, and create plans to overcome them. Adapts easily to changing priorities and direction based on new project learnings and team priorities. Demonstrated competency to effectively communicate (oral & written) cross-functionally with solid collaboration skills. Comfortable in client-facing situations and able to communicate complex topics clearly and simply. Excel in a startup environment, is excited to create new procedures and processes from scratch and has a strong entrepreneurial mindset. Be a problem solver, have a general manager mindset, and take the initiative to get the job done Possess strong planning, project management, and execution skills, and the ability to articulate where and how you have used them. Rigorous data-driven/analytical capability and ability and presence to present data effectively to a leadership team Work well in teams and cross-functional groups in a matrixed environment, both regionally and globally Possesses strong computer skills, including a high level of proficiency in MS Office, specifically Excel Authorization to work in the U.S. is required Ability to travel up to 50% of the time, including international travel and extended trips. NotCo is committed to fair and equitable compensation practices. The pay range for this role is $65,000 - $75,000. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

We Are: At Synopsys, we drive the innovations that shape the way we live and connect. Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration, empowering the creation of high-performance silicon chips and software content. Join us to transform the future through continuous technological innovation. You Are: You are a seasoned engineer with a passion for pushing the boundaries of technology. With 6 - 15 years of experience, you bring a wealth of knowledge in software architecture. You excel in C/C++ software development, digital simulation, compiler optimizations and your strong background in design patterns, data structures, and algorithms sets you apart. Your expertise in Verilog, SystemVerilog, coupled with your experience in Unix/Linux platforms, makes you a valuable asset. You are well-versed in developer tools like gdb and Valgrind. Your analytical and problem‑solving skills are top‑notch, and you are always eager to learn and explore new technologies. As a highly enthusiastic and energetic team player, you are ready to go the extra mile to achieve success. What You'll Be Doing: Designing, developing, and troubleshooting core algorithms for compiler. Collaborating with local and global teams to enhance runtime performance for verilog compiler. Engaging in pure technical roles focused on software development and architecture. Utilizing your knowledge of digital simulation flows and EDA tools to drive innovation. Leveraging your expertise in Verilog, SystemVerilog, and VHDL to develop cutting‑edge solutions. The Impact You Will Have: Driving technological innovation in chip design and verification. Enhancing the performance and quality of simulation tools used globally. Solving complex compiler optimizations problems to improve simulation performance. Collaborating with cross‑functional teams to achieve project milestones. Pioneering new software architectures that set industry standards. What You'll Need: Strong hands‑on experience in C/C++ based software development. Deep understanding of design patterns, data structures, algorithms, and programming concepts. Knowledge of ASIC design flow and EDA tools and methodologies. Proficiency in Verilog, SystemVerilog, and VHDL HDL. Who You Are: Highly enthusiastic and energetic team player with excellent communication skills. Strong desire to learn and explore new technologies. Effective problem‑solver with a keen analytical mind. Experienced in working on Unix/Linux platforms. Adept at using developer tools such as gdb and Valgrind. The Team You'll Be A Part Of: You will be part of the performance team in Digital Simulation. You will work closely with both local and global teams to drive technological advancements and achieve project goals. Rewards and Benefits: We offer a comprehensive range of health, wellness, and financial benefits to cater to your needs. Our total rewards include both monetary and non‑monetary offerings. Your recruiter will provide more details about the salary range and benefits during the hiring process. #J-18808-Ljbffr

Reports to: Managing Principle Mechanical Engineer, R&D Workplace Type: Hybrid, on-site in Santa Cruz an average of 4-days per week Capstan Medical:Creating a new standard for minimally invasive structural heart treatment Who we are: At Capstan Medical, we're driven by an unwavering commitment to transforming the treatment of heart valve disease. By merging surgical robotics with catheter-based technology and next generation implants, we've pioneered a patient-optimized approach to repair and replace heart valves. Our innovative technology offers a significantly less invasive alternative to traditional open-heart surgery while ensuring precise and reliable placement of the heart valve implant. With these advancements, we may be able to provide patients with a solution to their heart valve disease while significantly reducing recovery time and minimizing the risk of complications. With a dedicated team of heart valve device experts and robotics engineers, we are fully committed to developing a comprehensive and transformative solution that will positively impact the lives of individuals affected by this condition. Capstan Medical is uniquely positioned in Santa Cruz. This gives us access to the amazing technical talent of the Bay Area, but in an environment that we feel is conducive to doing our best creative work. Our office is adjacent to large tracts of open space with bicycle trails straight from the office doors offering access to the hills and beaches of Wilder Ranch State Park for road/mountain bicycle riding, hiking, and surfing. Come join us and become part of a team revolutionizing heart valve treatment! The Opportunity: We are building a novel medical robotic application, bringing together an exciting set of hardware and software into an elegant product. We are looking for someone who can take a mechanical system of the robot design from initial concept all the way to product. What You'll Do: Collaborate with Manufacturing and Clinical teams on designs, incorporating this input into quick and effective design iterations. Lead and set direction for system and subsystem architectures and mechanical design efforts while owning cross-functional mechanical deliverables and technical strategy Participate in building and bringing up prototype robotic systems and support all things mechanical in their pre-clinical lab use. Lead alignment of complex technical topics and hardware architecture across the Mechanical Engineering team and broadly across the R&D organization and Capstan. Document and communicate learnings on design manufacturability and reliability to the broader hardware team, mentoring others in best practices and scalable design approaches Document and communicate your work through design reviews and as appropriate released documents as part of the product development process Identify gaps and pitch in as needed to ensure that the team meets their goals and objectives, driving alignment across teams when priorities conflict Strengthen the team by providing leadership and mentorship on best practices and design strategies as they grow in their abilities to develop performant, scalable, and elegant designs. Be a valuable partner with feedback and collaboration in brainstorming and design reviews. What You'll Need: BS in Mechanical Engineering or related engineering discipline, or equivalent work experience Expecting 12+ years of relevant experience (medical device experience preferred) Comfort working with high levels of ambiguity and an ability to convert that into tangible outcomes Experience with designing, manufacturing transfer, and shipping of medical device capital equipment or equivalent complexity systems Deep expertise in areas particular to robotic system design: kinematics, mechanisms, bearings, gears, sensors, actuators. Experience with medical device (or equivalent) development process, design control, design verification, and regulatory processes Ability to work in a hybrid work environment, working onsite in Santa Cruz on average 4 days a week Ways To Stand Out: Experience with the full commercial lifecycle from concept through reacting to and addressing field issues with your designs. Skills with Python or Matlab for data analysis, simulation, and interacting with robotic equipment. Excessive nerdiness about manufacturing, mechanisms, robots, or any other adjacencies. Leadership experience. While this role is as an individual contributor, it is a position of significant technical and thought leadership within the company. Why Join Us: We offer a fun, fast-paced, collaborative environment where you will be working on transformational technologies in the cardiac healthcare space. We offer outstanding benefits with medical, dental, and vision covered at 100% for you and your family, as well as flex time off. We thrive in our work-hard, play-hard environment. Bring your bike or running shoes if you'd like or just be ready to enjoy a fun office outing. We enjoy time inside the office and out! We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, and disability, or other legally protected status. #J-18808-Ljbffr

Plant Breeding Technician 1 (CA) Quality Integrity Responsiveness Wish Farms is a nationally recognized year-round supplier of berries with growing regions throughout the USA, Canada, South America, and Mexico. With our committed focus on providing the best-tasting berries, Wish Farms continues to see impressive market growth. Established in 1922, we employ a dynamic group of passionate individuals who believe in our mission of providing the best tasting berries through living our core values of Quality, Integrity, and Responsiveness. We have a career opportunity available for a talented and motivated individual to join our team in Salinas, CA at our affiliated Berry Sweet Research organization as a Plant Breeding Technician. The Plant Breeding Technician will assist the Plant Breeder in all aspects of running the breeding program. The candidate will help set up and execute essential aspects critical to the success of the breeding program. Qualified individuals will need to have a strong background in horticulture and high degree of self-structure with the ability to perform successfully under minimal supervision. ESSENTIAL DUTIES AND RESPONSIBILITES: · Making crosses and harvest of resulting fruit and seeds · Treating seeds prior to planting · Manage a seed inventory and monitor satisfactory seed storage conditions · Sowing of seeds, transplanting, and care of seedlings in the lab, greenhouse and field · Collection of data on families and selections in the breeding program · Collect and organize fruit samples for storage, sensory, and other testing purposes · Manage postharvest data collection and data entry into breeding database · Label, organize and track plants/fruit/pollen/seeds accurately using QR codes and tablets · Supervise hourly labor as needed · Propagation of advanced selections · Assist in micropropagation and seed germinations in the lab · Maintain inventories and safe and sanitary conditions in the lab, greenhouse and field · Collect miscellaneous data relative to improving the functioning of the breeding program · Assistance with other related tasks as requested by management REQUIREMENTS: · Bachelor's degree in Horticulture, Agronomy, or similar Plant Science Preferred · Bilingual English/Spanish - Preferred · Strong communications skills, both oral and written · Basic computer skills with MS Word, Excel, and PowerPoint · Valid driver's license and occasional overnight travel required · Ability to work occasional weekends or holidays · Ability to work with hands and fingers, stand or walk, and capable of lifting 25 pounds This position is full time and offers a competitive benefits package including medical, dental, vision, life, and disability insurance as well as 401k with company match. Paid holidays & vacation too. To apply, please respond with your resume and a letter of interest on why you would like to join the team! Job Type: Full-time Pay: $71,000.00 - $85,000.00 per year Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Vision insurance Education: Bachelor's (Preferred) Experience: Farming: 1 year (Required) License/Certification: Driver's License (Required) Work Location: In person

Senior Scientist Santa Clara, CA Pay rate: $40+ an hour Our clients long-term vision is to use digital technology as part of a holistic approach to surgery across the episode of care to enhance surgical efficiency, promote better clinical outcomes and increase patient satisfaction. This position will serve as a scientific contributor for the development and execution of preclinical evidence strategies necessary to competitively position a product for domestic and international regulatory and clinical acceptance. Responsibilities Include · Leads and supports product evaluations involving animate, inanimate, and cadaveric models · Performs research supporting development of products or procedures in minimally invasive robotic surgery · Assisting or conducting investigations for medical device development and preclinical evidence generation aligned to R&D, Regulatory, and Commercial needs · Coordinate and ensure accurate documentation of laboratory activities · Conduct lab activities in compliance with USDA, AAALAC, and Animal use policies · Ensure compliance with 21 CFR Part 58 - Good Laboratory Practices · Contribute and support the design of appropriate studies to meet premarket and post market needs · Design, plan and execute preclinical animal studies for the assessment of safety, performance, and effectiveness Act as study coordinator in support of the Study Director Act as Study Director projects of varying levels of complexity · Assess, communicate, and manage the risks associated to the preclinical evaluation of products. · Assist in appropriate interpretation and dissemination of all evidence generated, based on evidence dissemination strategy, including study reports, abstracts, manuscripts, etc. · Demonstrate the ability to work effectively in a team-oriented environment that embraces ownership and accountability for innovation, change, risk, and flexibility · Build successful relationships internally and develop partnerships with key business partners Qualifications · A minimum of a bachelor's degree in Biological Science or a related discipline is required. Experience and Skills: · A minimum of 5 years of related scientific / technical experience within preclinical research is required. · Experience in preclinical science and processes along with an understanding of medical device development processes, related healthcare market environment, clinical trends, and preclinical regulations is required. · Track record of contributing to preclinical programs on time, within budget and in compliance to SOPs and regulations is required. · Experience working in a GLP environment and direct experience executing preclinical studies · Understanding of good documentation practices · Familiarity with animal welfare regulations and IACUC Preferred: · Experience working in Medical Devices or Robotics is preferred · Experience working with large animal models is desired · Experience in support of global regulatory submissions for medical devices, biologics, or drugs (including PMA/BLA/NDA and/or their global counterparts) is preferred.

Imagine what you could do here. At Apple, great ideas have a way of becoming great products, services, and customer experiences very quickly. Work at the forefront of innovation and bring new products and services to life. As an Operations Product Development (OPD) Design Intelligence Analyst you will engage with the Apple Engineering, Operations, Procurement, Marketing, and OPD Product Manager teams to help shape product design u0026 sourcing strategies that enable best-in-class hardware products. In this role you will identify existing and emerging technologies in the consumer electronics market and utilize your knowledge of hardware components, materials, and manufacturing design to investigate novel product and supply chain implementations. You will help influence product feature roadmaps by providing relevant engineering and cost analysis, and by identifying design, manufacturing, and sourcing opportunities. This position requires strong hardware engineering, materials, and manufacturing cost structures knowledge, as well as the ability to leverage interpersonal and communication skills. Ideal candidates will have a natural curiosity about how things work and why. Exceptional interpersonal u0026 communication skills Self-starter with strong sense of ownership u0026 robust organization skills Ability to resolve ambiguity through a creative yet data-centric approach to analysis/decision making Strong analytical skills and ability to maintain attention to detail within big picture thinking Experience managing multiple projects with competing priorities 7+ years of relevant experience in Operations, Manufacturing, Sourcing, Supply Chain or related area BS/BA in Engineering, Business, Supply Chain or a related field

About team We are the Engineering Architecture team of the PICO-Interactive Perception R&D Department. We are responsible for the architecture design and engineering implementation in the Interactive Perception Department. We focus on exploring the low-power consumption deployment of AI models, strive for excellence and aim to become an international team with leading technology. Responsibilities - Participate in research and development tasks to explore new frontiers in 3D Avatar generative models and deep dive into advanced 3D geometry, texturing, human reconstruction, and animation techniques. - Contribute to project discussions, offering innovative ideas for 3D modeling and avatar generation/animation. - Collaborate closely with XFN teams to refine 3D Avatar Generative models in business operations and transform advanced technology into PICO products. - Document research findings clearly and contribute to research publications, patents, and presentations. Minimum Qualifications: - Master's degree or above, majoring in Computer Vision, Computer Graphics, Mathematics, Game Design, Digital Arts, Animation, or related fields. - Keen interest in developing expertise in 3D modeling, texturing, and avatar generation. - Have solid research and practical experience in one or more fields, including but not limited to the following aspects: 3D face/head/hand/full-body modeling, editing, and driving; Explicit and implicit representations of the face/head/hand/full-body, such as NeRF, 3DGS, Codec Avatar; Generative modeling (e.g., Diffusion or Transformer models) for 3D/4D reconstruction/generation. - Proficient in algorithm design and implementation, with strong programming skills (e.g., Python/C/C++). - Hands-on experience with deep learning frameworks, preferably PyTorch. Preferred Qualifications: - Strong research ability with publications in top computer vision and graphics conferences and journals (such as CVPR, ICCV, ECCV, SIGGRAPH, SIGGRAPH Asia, NIPS, ICML, PAMI, IJCV, TOG, TVCG, etc.). - Good communication skills, capable of collaborating well with team members. - Self-motivated, with a strong thirst for knowledge, curiosity, and initiative, timely pay attention to and learn about the latest technologies in the industry, and is passionate about tackling technical challenges.

Grade 2 - PST meets minimum requirements and experience for client office and roving (with limited locations) positions, and patient service centers offering minimal services. Skill and comprehension level required for this category: Phlebotomy certification (where required) from an accredited agency, and a minimum of one year verifiable phlebotomy experience. Exhibit proficiency in blood collection by venipuncture and capillary technique from patients of all age groups, and urine drug screen collections. Able to grasp a firm understanding of the importance of compliance and safety as outlined during new hire orientation and annual training. Skill Requirements Administrative: Answer telephones, maintain logs/records, organizational skills, proficiency with numbers, research information, time management, use computerized databases, written and verbal communications. Machine: Personal computer. Physical Demands: Speech clarity, utilization of fingers and hands, standing-remaining on one's feet in an upright position, sitting-remaining in the normal seated position, handling-seizing, holding, grasping. Moderate physical effort (up to 30 pounds); must comply with applicable safety procedures. Working Conditions: Possible exposure to infection from disease-bearing specimens; regularly exposed to the risk of blood-borne diseases; must comply with applicable safety procedures. Vision Requirements: Far acuity-ability to see clearly at 20 feet or more; near acuity-ability to see clearly at 20 inches or less; depth perception-ability to judge distance and space relationships; color vision-ability to distinguish and identify different colors. License/Certification/Education: Requires a High School Diploma or equivalent with a minimum of one year of verifiable phlebotomy experience. Normally requires a Valid Driver's License along with a clean driving record. Job Description This position is NonExempt. Hours over 40 will be paid at Time and a Half. 1. Performs a variety of duties in the electrical, mechanical, electro-mechanical, chemical, or optical areas.; 2. Builds or assembles prototype materials, components, subassemblies and assemblies.; 3. Constructs, operates, troubleshoots, calibrates, adjusts, maintains and tests equipment, systems or products.; 4. Works from schematics, engineering drawings, and written or verbal instructions.; 5. Performs tests, analyzes data and writes reports; 6. Reviews or develops processing or manufacturing instructions.; 7. Maintains detailed documentation through all phases of development, testing and analysis.; 8. May assist in the transfer of technology and/or contribute in cross-functional discussions regarding device performance allegations. Two-year degree with 2+ years related experience or equivalent combination of education and technical work experience. May also require a license or certification in the area of expertise. Applies knowledge of technical concepts and practices, and a complete understanding of product or systems fundamentals in a functional area, and working knowledge of other related disciplines. Utilizes/interprets advanced numerical and statistical data and computer software programs to present documentation and analysis and resolve complex problems. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. (Cognitive Skills) Performs complex technical assignments usually without established procedures. Assists in the design, development, evaluation or modification of all area-specific equipment, materials, systems, and/or product. May determine types of tests or develop preventative maintenance plans assignments require considerable judgment, initiative, creativity and leadership in troubleshooting, suggesting alternatives, and making recommendations for continuous quality improvement methods. QualificationsEnter qualifications here Additional Information

At Tandem PV, we are a team of people who are passionate about building a more sustainable world by bringing cost effective solar panels onto the market. We're scaling metal-halide perovskite solar technology to make best-in-class mechanically stacked tandem modules. We have built efficient, durable cells, monolithic multi-cell submodules, and packaged modules with our scalable, low-cost process. Our next focus is expanding our team to work in our new pilot manufacturing facility. Job Summary: As a Durability Technician, you'll play a key role on the R&D team creating consistency in our testing processes, building set ups, and collecting data to feed back into the R&D process. This is a crucial next step in our growth and ability to scale as a company. To stand out in this role, you will: Build consistent testing hardware and software setups, then process small scale cells through those setups in a fashion that allows for clean data reads and outputs to the team. Maintain all wiring and assembly gear in a way that ensures cleanliness, consistent connection, and maintenance for long term use will result in clean data and usable metrology to confidently share our success with customers. Durability testing including lamination, edge seal cutting, glass cutting, cleaning, etc Throughout the durability process, we'll need you to maintain samples on durability tests; Pull samples and processing them as needed. Use various metrology techniques to measure samples, including : JV, EL, PL, Microscopy, etc. Qualifications We can teach a lot, but there are some basics you'll need to know to hit the ground running, that includes: Experience with electronics in testing environments Experience maintaining and troubleshooting processing tools Hands on lab experience - including knowledge of safety in a wet chemistry environment and safe use of hazardous materials Key skills that will help you accelerate in this role include: A creative and curious approach to problem solving Systems thinking - seeing each part/piece as a part of something bigger, piecing everything together for smooth connections and handoffs. Verbal and written communication skills are crucial - they also make for a safer and more efficient environment If you happen to have these skills- it'll put you ahead of the game! Python programming experience Experience working in a solar company What we offer: An awesome team of dedicated technologists changing the way the world is powered! If that's not enough, we'll take good care of you and your family with: Flexible PTO Healthcare coverage Life Insurance Long-term & Short-term Disability Parental leave Meaningful equity Tandem PV uses perovskite & silicon mechanically-stacked tandems to upgrade silicon solar panels, sharply decreasing installed systems costs, significantly increasing module manufacturing profit margins, and opening up vast new solar markets in the US and worldwide. TPV was co-founded by Stanford PhDs Colin Bailie and Chris Eberspacher; is advised by industry experts from Corning, First Solar, Vivint Solar, and Kateeva; has raised more than $50M in Series A funding. We were recently recognized as the Best Pre-Commercial Venture of 2025 by the Industry Growth Forum (IGF) We are a team of people who are passionate about building a more sustainable world by delivering a new generation of solar panels to the market. We are constantly growing and are always looking for dedicated, hardworking, and empathetic teammates. Tandem PV is an equal opportunity employer. All qualified applicants are encouraged to apply.

We exist to create positive change for people and the planet. Join us and make a difference too! BSI Consulting Services is a trusted and agenda-shaping partner providing 'best practice' technical, regulatory, and business expertise and intelligence for our clients' most critical EHS, Supply Chain, and Digital risks and opportunities to achieve greater resilience, impact, and future-readiness. About the role: BSI is looking for a strong, technical Certified Industrial Hygienist (CIH) to join our dynamic EHS team in the Northern California area. The ideal candidate will have 5-7 years of hands-on IH experience, with the proven ability to independently perform exposure assessments, plan and execute sampling strategies, and analyze and report results using sound statistical methods. You'll be supported by a collaborative team and enjoy comprehensive benefits while helping world-class clients enhance their safety and environmental practices. Key Responsibilities: * Perform technical industrial hygiene assessments, including air, noise, and chemical sampling. * Plan and execute exposure monitoring studies, selecting appropriate methodologies and equipment. * Conduct data analysis and statistical evaluation of sampling results; prepare detailed, defensible reports with actionable recommendations. * Manage laboratory inspections, document unsafe conditions, and collaborate with staff to develop JHAs and identify project-specific risks. * Lead incident investigations and implement corrective actions to ensure continuous improvement in safety performance. * Provide general EHS technical support and guidance to a variety of clients * Developing and delivering EHS/Occupational Health and Safety training * Conduct EHS assessments/general program compliance audits * Stay current and ensure compliance with federal, state, and local EHS regulations To be successful in this role, you will have: * Bachelor's degree in Industrial Hygiene, Occupational Health, Environmental Science, or a related field. * 5-7 years of technical IH experience, preferably in consulting or laboratory environments. * Demonstrated ability to independently perform sampling, plan studies, conduct assessments, and complete statistical reporting. * Experience conducting risk assessments and accident investigations. * Excellent written and verbal communication skills, with experience preparing client-ready reports. * Proficiency in Microsoft Office; experience with IH data tools and statistical software is a plus. * Required certification: CIH * Preferred additional certifications: ASP, CSP, AEP, CPE, or CHMM (not required, but highly valued). What we offer: BSI offers a competitive salary, group-sponsored health and dental, short-term and long-term disability, a company-matched 401k plan, company paid life insurance, 11 paid holidays and 4 weeks paid time off. The salary for this position can range from $98,400 to $135,300 annually; actual compensation is based on various factors, including but not limited to, the candidate's competencies, level of experience, education, location, divisional budget and internal peer compensation comparisons. #LI-MA1 About Us BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives. Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments. Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs. Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world. BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: R&D Operations Job Sub Function: Product Development Testing Job Category: Business Enablement/Support All Job Posting Locations: Santa Clara, California, United States of America Job Description: Johnson & Johnson is hiring for a R&D Technician II - Shockwave Medical to join our team located in Santa Clara, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************/. Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that's pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque. Position Overview The R&D Technician II will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases. The R&D Technician II will participate on multiple cross-functional development teams that manage projects from concept through commercialization. Perform and support a variety of development and engineering activities, which mainly focus on disposable devices prototyping, fabrication and testing. Will work directly with other R&D technicians and R&D engineers to complete duties described below. Essential Job Functions Generate functional prototype from design concepts and assist the transfer of R&D product build to manufacturing Support product builds through all R&D project phases, providing feedback on assembly process Assist other technicians, assemblers and engineers on procedures and product assembly Assist engineers with product and process development and improvement Perform testing to support design, process, and equipment validation Prepare test samples (products/materials/solutions) for routine and qualification testing Support the build and assembly of prototypes Identify issues as they arise and assist in troubleshooting of procedures and/or instruments Maintain accurate documentation of concepts, designs, drawings, and processes Other duties as assigned Requirements High School Diploma with 2+ years' technician experience or 3 years' other relevant hands on medical device experience Experience with balloon catheter, hydrophilic coating, or other cardiovascular medical devices development preferred Ability to perform work under a microscope. Experience with test method execution is a plus Familiar with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and laboratory practices Ability to work in a fast-paced environment while managing multiple priorities Comfortable working in a clean room environment Ability to communicate effectively Experience with MS Office Employee may be required to lift objects up to 25lbs Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via *******************/contact-us/careers or contact AskGS to be directed to your accommodation resource. Required Skills: Preferred Skills: The anticipated base pay range for this position is : $22.67 - $36.24 Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company's long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation -120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year Holiday pay, including Floating Holidays -13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave - 10 days Volunteer Leave - 4 days Military Spouse Time-Off - 80 hours Additional information can be found through the link below. *********************************************

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: R&D Operations Job Sub Function: Product Development Testing Job Category: Business Enablement/Support All Job Posting Locations: Santa Clara, California, United States of America Job Description: Johnson & Johnson is hiring for a R&D Technician II - Shockwave Medical to join our team located in Santa Clara, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************/. Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that's pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque. Position Overview The R&D Technician II will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases. The R&D Technician II will participate on multiple cross-functional development teams that manage projects from concept through commercialization. Perform and support a variety of development and engineering activities, which mainly focus on disposable devices prototyping, fabrication and testing. Will work directly with other R&D technicians and R&D engineers to complete duties described below. Essential Job Functions Generate functional prototype from design concepts and assist the transfer of R&D product build to manufacturing Support product builds through all R&D project phases, providing feedback on assembly process Assist other technicians, assemblers and engineers on procedures and product assembly Assist engineers with product and process development and improvement Perform testing to support design, process, and equipment validation Prepare test samples (products/materials/solutions) for routine and qualification testing Support the build and assembly of prototypes Identify issues as they arise and assist in troubleshooting of procedures and/or instruments Maintain accurate documentation of concepts, designs, drawings, and processes Other duties as assigned Requirements High School Diploma with 2+ years' technician experience or 3 years' other relevant hands on medical device experience Experience with balloon catheter, hydrophilic coating, or other cardiovascular medical devices development preferred Ability to perform work under a microscope. Experience with test method execution is a plus Familiar with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and laboratory practices Ability to work in a fast-paced environment while managing multiple priorities Comfortable working in a clean room environment Ability to communicate effectively Experience with MS Office Employee may be required to lift objects up to 25lbs Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via *******************/contact-us/careers or contact AskGS to be directed to your accommodation resource. Required Skills: Preferred Skills: The anticipated base pay range for this position is : $22.67 - $36.24 Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company's long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation -120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year Holiday pay, including Floating Holidays -13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave - 10 days Volunteer Leave - 4 days Military Spouse Time-Off - 80 hours Additional information can be found through the link below. *********************************************

Job Details:Job Description: Altera is a global leader in FPGA (Field-Programmable Gate Array) semiconductor solutions, enabling innovation in embedded computing and programmable logic. Our Finance team at Altera plays a critical role in shaping strategy, driving profitability, and supporting growth in a dynamic, high-tech environment. Position Overview The R&D Financial Specialist will support R&D expense management, financial planning, forecasting, and analysis for Altera's semiconductor business. This role partners with cross-functional teams-including Engineering, Sales, Operations, and Product Management-to provide insights that influence strategic decisions and optimize financial performance. Key Responsibilities R&D Ownership & Reporting Consolidate and report short- and long-term R&D results. Analyze revenue, cost structure, margins, and profitability trends. Support quarterly and annual financial close processes ensuring accuracy. Forecasting & Budgeting Develop financial models for revenue forecasting, cost analysis, and operating expenses. Assist in annual budgeting and strategic planning processes. Identify key business drivers impacting financial performance. Business Performance Analysis Conduct variance analysis (actual vs. forecast) and provide actionable recommendations. Support pricing strategies, product profitability analysis, and investment decisions. Cross-Functional Collaboration Partner with Engineering, Sales, Operations, and Product teams to align financial goals with business strategies. Provide financial insights for executive decision-making and strategic initiatives. Salary Range The pay range below is for Bay Area California only. Actual salary may vary based on a number of factors including job location, job-related knowledge, skills, experiences, trainings, etc. We also offer incentive opportunities that reward employees based on individual and company performance. $113.7K - $164.7K USD We use artificial intelligence to screen, assess, or select applicants for the position. Qualifications: Qualifications Bachelor's Degree in Finance, Accounting, Economics, or related field (MBA or CPA preferred). 3+ years of experience in FP&A, P&L management, or corporate finance-preferably in semiconductor or technology industry. Strong knowledge of financial modeling, forecasting, and variance analysis. Proficiency in financial tools such as Oracle, Hyperion, Power BI, and advanced Excel. Excellent communication and collaboration skills; ability to work in a fast-paced environment with a can-do perspective. Job Type: RegularShift:Shift 1 (United States of America) Primary Location:San Jose, California, United StatesAdditional Locations:Oregon HillsboroPosting Statement:All qualified applicants will receive consideration for employment without regard to race, color, religion, religious creed, sex, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, military and veteran status, marital status, pregnancy, gender, gender expression, gender identity, sexual orientation, or any other characteristic protected by local law, regulation, or ordinance.

On-Site **Research and Development Chemist (Senior)** Initiate, design, execute testing and interpret data for the development of industrial energetic products. Conduct exploratory research and synthesis to further existing knowledge or produce new knowledge and add to the development of potential products. Perform chemical analyses of various materials and chemicals. Broaden the knowledge base of state-of-the-art principles and theories. Skills including, but not limited to: + Ability to communicate difficult concepts and negotiate with others to adopt practical and applicable solutions to Research and Development (R&D) challenges in the energetics field. + Interface with engineering, safety and the production staff to lead functional teams or projects with moderate resource requirements, risk, and/or complexity. + Mentors lower-level chemists. + Demonstrate safety related energetic materials practices. + Collaborate with engineering associates in support of product function related investigations. + Ability to solve complex problems and take a broad perspective to introduce innovative solutions. + Interface with powder processing for the manufacture/scale-up of existing or new R&D materials. + Determine needs and prepare CARs and other documentation related to new (instrumentation and equipment) purchases. + Review and edit reports, presentations and other documents related to engineering, manufacturing and/or chemistry activities, including technical test plans and reports. + Generate white papers and support proposal preparation. + Proficient in the use of all laboratory instrumentation and operations. + Maintain a working knowledge of powder processing operations and testing requirements. + General understanding of engineering and test protocols related to ordnance operations. + Perform independent chemical research and development. + Conduct non-routine analyses that may require procedural modifications. + 25% travel requirement in support of R&D expansion. **Education Required** : + BS, MS or Ph.D. in chemistry or technical discipline **Experience Required:** + Experience in a technical and manufacturing environment in the aerospace/defense industry (7+ years of experience with a BS degree, 4+ years of experience with an MS degree, or 1+ years of experience with a Ph.D.); + ordnance experience is required. + Polymer chemistry experience is a plus. \#LI-JW2 **Ralliant Corporation Overview** Ralliant, originally part of Fortive, now stands as a bold, independent public company driving innovation at the forefront of precision technology. With a global footprint and a legacy of excellence, we empower engineers to bring next-generation breakthroughs to life - faster, smarter, and more reliably. Our high-performance instruments, sensors, and subsystems fuel mission-critical advancements across industries, enabling real-world impact where it matters most. At Ralliant we're building the future, together with those driven to push boundaries, solve complex problems, and leave a lasting mark on the world. **About PacSci EMC** Pacific Scientific Energetic Materials Company (PacSci EMC), a Ralliant Corporation (NYSE: RAL) operating company, makes critical missions possible. From concept to demonstration to delivery, we provide leading-edge energetic materials, devices and subsystems for use in military and commercial applications. With engineering and manufacturing capability in Arizona and California, our associates work together to solve the toughest technical challenges with a dedication to Safety First, Quality Every TimeTM. We enable success for innumerable missions on a daily basis, impacting the lives of military personnel, law enforcement officers, commercial airline pilots, astronauts, and oil field operators. For nearly a century, PacSci EMC's experience and expertise has been relied upon in the times When Milliseconds MatterTM. For more information, go to ******************** EMC is an equal opportunity employer. We do not discriminate against any applicant or employee on the basis of race, sex, religion, age, national origin, color, disability, or veteran status. Nonetheless, pursuant to our subcontractor status on highly sensitive national security matters, Mechanical Assemblers and all other floor personnel who frequently shift cell assignments, as well as any personnel directly working with the following contract are subject to the following contractual provision: THAAD PRIME Flowdowns (H-Clauses) H-42 FOREIGN PERSONS, paragraph D., "All employees of all entities that make up the Contractor's team, whether subcontractors, consultants, or anyone who works with or on behalf of the Contractor will be citizens of the U.S." Accordingly, only U.S. citizens will be qualified to fill these roles. We are committed to providing a workplace free of any discrimination or harassment. We all have a role in building a community where everyone belongs. Where you can speak your mind, be yourself, and feel supported. It's how we achieve more together - for each other, for our customers, and for the world. ******************************************** We Are an Equal Opportunity Employer. Ralliant Corporation and all Ralliant Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Ralliant and all Ralliant Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at applyassistance@Ralliant.com. **Bonus or Equity** This position is also eligible for bonus as part of the total compensation package. **Pay Range** The salary range for this position (in local currency) is 101,500.00 - 188,500.00 **Is this role subject to ITAR?** The essential duties of this position require adherence to U.S. Government export control regulations. Accordingly, candidates must either be U.S. Persons (i.e., U.S. citizens, U.S. lawful permanent residents, or protected individuals as defined by 8 U.S.C. 1324b(a)(3)) or be prepared to collaborate with the company in securing the necessary U.S. government export authorizations. While the company encourages all interested applicants to apply, please be aware that ongoing employment is dependent upon obtaining the appropriate government export authorizations.

Research and Development Chemist (Senior) Initiate, design, execute testing and interpret data for the development of industrial energetic products. Conduct exploratory research and synthesis to further existing knowledge or produce new knowledge and add to the development of potential products. Perform chemical analyses of various materials and chemicals. Broaden the knowledge base of state-of-the-art principles and theories. Skills including, but not limited to: Ability to communicate difficult concepts and negotiate with others to adopt practical and applicable solutions to Research and Development (R&D) challenges in the energetics field. Interface with engineering, safety and the production staff to lead functional teams or projects with moderate resource requirements, risk, and/or complexity. Mentors lower-level chemists. Demonstrate safety related energetic materials practices. Collaborate with engineering associates in support of product function related investigations. Ability to solve complex problems and take a broad perspective to introduce innovative solutions. Interface with powder processing for the manufacture/scale-up of existing or new R&D materials. Determine needs and prepare CARs and other documentation related to new (instrumentation and equipment) purchases. Review and edit reports, presentations and other documents related to engineering, manufacturing and/or chemistry activities, including technical test plans and reports. Generate white papers and support proposal preparation. Proficient in the use of all laboratory instrumentation and operations. Maintain a working knowledge of powder processing operations and testing requirements. General understanding of engineering and test protocols related to ordnance operations. Perform independent chemical research and development. Conduct non-routine analyses that may require procedural modifications. 25% travel requirement in support of R&D expansion. Education Required: BS, MS or Ph.D. in chemistry or technical discipline Experience Required: Experience in a technical and manufacturing environment in the aerospace/defense industry (7+ years of experience with a BS degree, 4+ years of experience with an MS degree, or 1+ years of experience with a Ph.D.); ordnance experience is required. Polymer chemistry experience is a plus. #LI-JW2

Job Description Title: Senior R&D Technician Status: Full-time, hourly Reports to: Principal Engineer About the Role VahatiCor is seeking a hands-on R&D Technician with 5+ years of experience to support development of next-generation catheter and interventional devices. This individual will perform in-house R&D testing, build prototypes, maintain lab equipment, and assist engineers in process and product development activities in a fast-paced environment. Key Responsibilities • Support engineers in prototyping, assembly, and testing of catheter and interventional devices. • Prepare and set up test fixtures, equipment, and instruments for R&D evaluations. • Executes equipment calibration, preventive maintenance, and installation qualification • Execute test protocols, record data accurately, and maintain laboratory notebooks and logs. • Assist with development and refinement of test methods and fixtures. • Help maintain laboratory equipment, tools, and work areas in safe and calibrated condition. • Perform in-process inspections and measurements to support design and process evaluations. • Partner with engineers to troubleshoot, document, and resolve technical issues. • Support preparation of reports, data summaries, and technical documentation. • Provide support and guidance to junior technicians and build operators/assemblers. Qualifications • Associate's degree in engineering technology preferred, or equivalent technical training. • 5+ years of hands-on experience in medical device R&D, process development, or testing environment. • Proficiency in MS Word and MS Excel for basic data analysis, tracking, and clear written communication. • Familiarity with catheter or interventional devices strongly preferred. • Strong understanding of test equipment, measurement tools, and laboratory practices. • Comfortable with mechanical assembly, equipment repair, inspection tools (microscope, calipers, etc.), and handling delicate parts. • Strong organizational and documentation skills; attention to detail. • Ability to work collaboratively in a dynamic environment. Eligibility Candidates must be permanently authorized to work in the United States without the need for current or future visa sponsorship. We are currently unable to sponsor employment visas or permanent residency (PERM) applications. Location & Compensation This is an onsite role based in Santa Clara, CA, and is open to candidates living within a reasonable commuting distance of our office. At this time, we are not considering applicants who would need to relocate, either within or outside of California. There is no relocation package available. Salary ranges are based on San Francisco Bay Area market data. Actual compensation offered may vary depending on factors such as experience, skills, qualifications, and abilities relevant to the role, as well as the geographic location of the individual hired. The anticipated hourly rate for this position is $41.68 - $56.40. Please note that the top of the range is reserved for candidates who demonstrate exceptional qualifications and experience directly aligned with the requirements of the role. Most candidates should expect to receive an offer within the mid-range of the posted range, based on these considerations. Equal Employment Opportunity Statement VahatiCor is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Employment decisions are based on qualifications, merit, and business needs. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status. Third-Party Recruiter Notice We do not accept unsolicited resumes from staffing agencies or recruiters without a signed agreement in place. Resumes submitted without an agreement will be considered property of VahatiCor, and no fees will be paid if the candidate is hired. Agencies may email ******************* for formal submission arrangements.