Research and development technician jobs in Monterey, CA - 101 jobs

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.

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

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.

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.

Oxford BioTherapeutics (OBT) is a dynamic, rapidly-growing, international biotechnology company based in Oxford, UK, and San Jose, CA. We are a clinical-stage oncology company with a pipeline of immunooncology and antibody-drug conjugate-based therapies. OBT's IO (Immuno-Oncology) discovery process provides unique insight into the cancer-immune cell synapse and has identified several novel IO candidates for cancer therapy. Discovery of novel tumor antigens and immune cell surface proteins at OBT is performed using the proprietary Oxford Genome Anatomy Project (OGAP) database. OBT currently has one ADC in phase 1b clinical trials in collaboration with Menarini, and target discovery collaborations with Boehringer Ingelheim, Zymeworks and Roche. Purpose of this Role: OBT is seeking an experienced, creative and motivated scientist to contribute to our company's Discovery Biologics Protein Science group. Work independently, and in a matrix, to lead the development of antigen antibodies against novel targets discovered by Oxford Biotherapeutics, headquartered in the UK. The successful candidate will be involved in multiple aspects of the production of recombinant proteins, monoclonal antibodies, multi-specific scaffolds, and novel protein modalities to enable all aspects of Early Discovery and Validation Research. Roles & Responsibilities: Be a contributor to the discovery and development of antibody therapeutics for oncology and immune oncology for novel targets. Support recombinant protein and bi- and multi-specific antibody discovery plans (immunogen design, assay development, screening, and functional characterization methods) Support biological discovery through different platforms of protein and antibody discoveries. Responsible various target projects to execute protein production and antibody discovery/optimization in various platforms Generate target over-expressing cell lines for antibody discovery work Develop strategies to express, purify, and analyze proteins for novel tumor targets expressed in mammalian cells. Perform purification using AKTA/HPLC systems and maintain equipment. Conduct antibody characterization of antibodies including binding affinity and binding kinetics through Octet/Biacore, epitope binning/mapping, and functional assays. Troubleshoot experimental issues with guidance; contribute to process and assay transfers. Mentor lower-level colleagues and assist in scientific optimization & development. Analyze data, interpret results, identify problems, and develop trouble-shooting plans Maintain accurate documentation and follow laboratory safety procedures. Knowledge of the biologics drug discovery process and representation of the protein science function at project team meetings. Compliances with data management, laboratory notebook policy, and laboratory safety. Knowledge, Experience, and Skills: Requirements: Ph.D. in biological sciences or related fields with 4+ years of post-Ph.D., or MS with 6+ or BS with 8+years of experience in biopharma industry or closely related scientific discipline, preferably in a fast-paced startup environment. Experience in molecular biology or/and biochemistry, including gene manipulation, subcloning, expression vector modifications, and protein expressions in HEK & CHO cell systems Experience in developing and optimizing recombinant proteins and bi- and multi-specific antibody formats across multiple parameters is preferred. Extensive experience in human protein and antibody purification techniques, including affinity chromatography, ion exchange chromatography (HIC), ion exchange chromatography (IEX), and size exclusion chromatography (SEC). Proficiency in operating and troubleshooting modern chromatography hardware and software, such as Cytiva AKTA systems and Agilent HPLC and UPLC. Preferred: Antibody drug discovery experience for immune oncology in biopharmaceutical industry is a plus. Ability to independently manage projects and deliver results on stringent timelines with high quality is plus Oneofourtopprioritiesistomaintainthehealthandwellbeingofouremployeesandtheirfamilies.Toachievethisgoal,weoffercomprehensivebenefits. BenefitsOffered: Medical,dentalandvisioninsuranceforemployeeanddependents FSA(FlexibleSpendingAccount) STD,LTD,BasicLifeandAD&DInsurance,SupplementalLife 401(k) Plan 120hoursofPaidTimeOff 5sickdaysperyear 11public holidays EmployeeReferralBonusProgram Annualbonusprogram Newhirestockoptions EqualOpportunitiesStatement OBT is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status, and veteran status. All qualified applicants will receive consideration for employment. One of our top priorities is to maintain the health and wellbeing of our employees and their families. To achieve this goal, we offer comprehensive benefits WhyJoinUs We promote a culture of innovation, responsibility, and steadfast commitment to our goal.Together, we believe we can pool our resources and our uniqueness to develop novel, robust cures for one of the most challenging health conditions today. We recognize that our team is only as good as the people in it.Our people have used the words friendly, collaborative, and hard-working to describe the culture here at OBT. Above all, we trust each other. This is why, while we strive to ensure that we hire only the best people to meet our goal, we also strive to provide a working environment that is based on cooperation, innovation, and mutual respect.

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

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $56,700.00 - $93,300.00 Position Summary: The Research and Development (R&D Science) group at ProteinSimple, a Bio-Techne brand, is seeking an inquisitive and motivated Advanced Research Associate to join our growing team on our mission to develop game-changing analytical instrumentation. As a part of the Product Development Team, you will work among innovative and supportive scientists and engineers that have a passion for product development and a knack for disrupting the way people typically characterize their samples. Our team works on exciting technologies for analysis of biomolecules and cells, including capillary electrophoresis, automated immunoassays, microfluidics, and cell sorting. In this role, you will be involved in product development from early concept to commercialization for ProteinSimple products through assay optimization and validation, with the goal of delivering cutting edge technologies to our global customer base. If you have experience with analytical instruments, assay development, or capillary electrophoresis - this might be the role for you. If you want to make better analytical tools to enable our customers to make better medicines, apply today. Key Responsibilities: Work closely with scientists from diverse backgrounds to learn and develop new analytical assays and reagents Design, execute, and optimize experimental plans and protocols Analyze, interpret, and troubleshoot results Document and present experimental results to project and department team members Participate in technical discussions and team meetings Technical ownership for various study types (e.g., stability, verification, and validation) Collaborate with hardware and software engineers during development Participate in technical transfer of products from Product Development to Manufacturing Help train new employees as needed Education and Experience: BS (with 5-8 years industry experience) or MS (with 2-5 years industry experience) in analytical chemistry, biotechnology, biochemistry, molecular biology, or related field Experience working in a biotechnology, pharmaceutical, CRO, or CDMO company is preferred Knowledge, Skills, and Abilities: Hands-on experience with biomolecule characterization technique is required (e.g., LC, Octet, cIEF, CE-SDS, DLS, etc.) Experience running capillary electrophoresis is strongly preferred Experience running Maurice instrument is strongly preferred Experience with biotechnology assay development is a plus Eagerness to learn innovative analytical platforms and contribute to their advancement Creative and critical thinker with careful execution of experiments Ability to quickly learn and thoughtfully apply new skills and procedures Desire to grow with a fast-paced and highly collaborative team Must have strong organizational skills with high attention to detail Must have good verbal and written communication skills Strong team player and self-starter with the ability to work independently and collaboratively Ability to prioritize own work and manage time efficiently for project deadlines, with flexibility to changing priorities Experience performing verification and validation studies is a plus Must be proficient in MS Office (Excel, Powerpoint, Word). Experience with JMP statistical software and/or a programming language (Python, MATLAB, R etc.) is preferred. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. 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. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

The Media Analytics Department at NEC Labs America solves fundamental challenges in computer vision, with a focus on autonomy, embodied AI, LLM agents and foundational vision-language models. We are seeking research engineers with skills and experience in developing autonomy and robotics stacks (sensors, perception, navigation, planning, control, or simulation). This unique position offers the opportunity to work closely with our research team to transform breakthrough ideas into practice. Besides helping build innovative autonomy solutions from the ground up, the position offers the opportunity to publish at top-tier venues such as CVPR or ICCV. To check out our latest work, please visit: **************************************************

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 Product Development Job Sub Function: Biomedical Engineering Job Category: Scientific/Technology All Job Posting Locations: Milpitas, California, United States of America, Mountain View, California, United States of America, Palo Alto, California, United States, San Francisco, California, United States of America, San Jose, California, United States of America, South San Francisco, California, United States of America, US356 CA Santa Clara - 5303 Betsy Ross Drive Job Description: Johnson & Johnson is hiring for a Principal R&D Engineer (Balloon Technology) - 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 Principal R&D Engineer (Balloon Technology) will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases. The Principal R&D Engineer will participate on multiple cross-functional development teams that manage projects from concept through commercialization. They will support product development efforts in our IVL balloon related devices as well as develop new balloon technologies to address the anticipated needs of future applications. Essential Job Functions Provide technical leadership for projects including managing technology development teams Design and develop product(s) in compliance with the company's Design Control requirements and consistent with applicable regulatory requirements. Partner with the Adv. R&D and PDP teams to translate finished device requirements to the balloon component level Survey emerging technologies in the balloons and polymer science space and explore novel applications to support company strategic goals Identify practical ways to apply new balloon/polymer technologies to improve current and next generation products Execute a long-term strategy with Technologies Development Team for examining new designs, materials as well as processing methods for next-generation balloon concepts Prototype and develop proof of concept designs, disease models and test methods of testing these concepts in a simulated environment and develop new product designs based on the defined user needs. Work with clinical and scientific advisors as well as Key Opinion Leaders in translating clinical needs into design solutions while utilizing these resources to develop and optimize product design. Analyzes, evaluates, sources, and coordinates the procurement of new materials to support prototyping and pilot operation as well as to maintain relationships with suppliers to ensure the delivery of superior components and services. Participate as SME or core team member on product development team(s) that manage projects from concept through commercialization. Responsible for ensuring proper documentation (e.g., component and assembly drawings) consistent with company's quality system. Responsible for knowing and planning activities consistent the company's quality policy and quality objectives. Develop protocols/reports and perform product in-vitro, in-vivo as well as verification and validation testing. Enhance the intellectual property position of the company via invention disclosures and patent applications. Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to company's products. Support company goals and objectives, policies and procedures, Quality Systems, and FDA regulations. Other duties as assigned. Qualifications Bachelor's Degree in Mechanical Polymer Science or other relevant engineering/technical degree and 10 years' experience in the medical device industry or a Master's Degree and 8 years' experience in medical devices. 3+ years of experience in polymer product development including experience with balloon blow molding. Knowledge of disposable peripheral and coronary device design, material selection, and testing. Strong understanding of engineering materials, component selection, and design for reliability and manufacturability. Proven track record in technology development and/or early-stage R&D; capable of planning and executing tasks for progressing towards a loosely defined research goal. Proven successful project leadership skills. Effective communication skills with all levels of management and organizations. Ability to operate independently and adaptability to changing requirements. Ability to work in a fast-paced environment, managing multiple priorities. Previous experience managing cross functional teams is preferred. Proficiency in SOLIDWORKS and Design of Experiments is a strong plus. Employee may be required to lift objects up to 25lbs. Additional Information: The anticipated salary range for this position is $141,000 - $227,700. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis. Employees and/or eligible dependents may be 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. Employees may be 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. Employees are eligible for the following time off benefits: Vacation - up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year Holiday pay, including Floating Holidays - up to 13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Additional information can be found through the link below. ********************************************* The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. · Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit ******************** The anticipated base pay range for this position is : $141,000 - $227,700 Additional Description for Pay Transparency: The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis.

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Job Description AccuraGen is seeking a dedicated Research Associate to join our innovative team. In this role, you will support various research projects focusing on assay development and clinical validation. You will assist in experimental design, data collection, and analysis while collaborating with scientists to advance our MRD assay. Responsibilities: Receive and process specimen shipments Prepare samples for routine testing and analysis Conduct testing under supervision of a senior staff Perform routine technical procedures and functions according to departmental Standard Operating Procedures Contribute to molecular biology and genomics workflow development and improvements Ensure accurate and consistent recording of experiment methods, materials and results; keep a high-quality laboratory notebook Monitor, operate and troubleshoot equipment to ensure proper functionality Maintain a clean, orderly, and safe lab environment Assist with safety, hazardous waste, and facilities Demonstrate the ability to make technical decisions regarding testing and problem solving Perform other duties as needed Adjust work schedule to meet time-sensitive project milestones Requirements Qualifications: Bachelor's degree in a life science or equivalent One year of experience working in a lab setting Knowledge of basic laboratory safety and protocol Skilled in working with basic laboratory equipment Strong understanding of standard molecular biology techniques (such as PCR, gel electrophoresis, and DNA/RNA isolation) Proficiency with basic computer skills, including data entry, spreadsheets, and document preparation Preferred Qualifications: Experience in a research laboratory setting. Experience with next-generation sequencing (NGS) technologies. Benefits Health Care Plan (Medical, Dental & Vision) Retirement Plan (401k, IRA) Paid Time Off (Vacation, Sick & Public Holidays)

Kettmann Machining, Inc is looking for an experience R&D Engineer/Programmer that specializes in Machining. This person would be customer facing on any new product needs within the medical device space of existing customers and be able to advise based on design for manufacturability. Job scope: Closed job review of all New Products (validation of the build plan against the actual manufacturing method) Establishing of build plan through a Job Traveler Communication of customer requirements to the job traveller, work instructions and customer drawing approval of customer change requests in accordance with Company Policy and Procedures Verification of manufacturing sequence Mill programming experienced preferred ESPRIT software experience preferred but not required

Align Technology is the industry leader and innovator in medical devices which focuses on revolutionizing the digital dental and orthodontic industry. Align Technology is looking for an R&D Engineer III, Core Product for our San Jose, CA office. This exciting new role would be part of a culture that is helping to improve lives every day through digital dentistry. The R&D Engineer III, Core Product candidate should have exceptional skills with product research and development in the medical device industry. The R&D Engineer III, Core Product will be the lead engineer responsible for planning, leading, and executing projects focusing on product design and design improvement. They will work closely with internal and external resources in a multidisciplinary team working with materials, software, and manufacturing to conduct research and development in the areas of product performance, design, and improvement. This role will be part of Align Technology's goal to deliver our clear aligners (Invisalign) to our customers. * Lead product development projects and research projects until product launch * Work independently to develop and evaluate new products and solutions and adapt and improve existing ones * Design and evaluate product prototypes with biomechanical test models and experimentation * Design, build, and verify test hardware, software, and systems as needed * Define and conduct procedures for bench top testing to evaluate product performance, including efficacy, reliability, verification, and validation * Work with clinical team to conduct pilot studies and other investigations * Simulate real world conditions and measure outputs using sensors * Collaborate with diverse, cross-functional teams to incorporate design and features into prototypes * Understand and master complex systems with sound mechanical principles * Define procedures to evaluate product performance and conduct bench top testing * Responsible for ensuring that testing covers efficacy, reliability, verification, and validation * Perform statistical data analysis and interpretation * Perform and document work in accordance with FDA/ISO regulations, including test protocols, test results, and other requirements * Collaborate with manager and cross-functional team in creating product and test plans * Communicate with professionals in the field at all levels and transition information into product improvement * Conceive new product and technology development plans * Work in a fast-paced environment and meet critical deadlines * Problem-solve issues with attention to detail * Provide general engineering support in R&D

JOB SUMMARY: Progressively initiate, coordinate and implement research and development projects focusing on seed diagnostic biology, seed production and enhancement technology, in order to improve seed physiological quality at Sakata Seed America. ESSENTIAL DUTIES AND RESPONSIBILITIES: Primary responsibility includes responsible for designing, implementing and analyzing multi-disciplinary research experiments aimed at improving seed and seedling physiological quality in the company. This advanced level technical position will be responsible for developing and implementing new technologies and further refining the existing protocols that would enhance physiological quality of stock and commercial seed. Design and conduct multiple research and development projects in an organized and timely manner, as requested by QA, R&D, Marketing, Supply Chain Departments. Understand the dynamic business requirements and transform them into short-term and mid-term research projects. Responsible for data analyses of results obtained in internal and external projects and subsequent decision making, including oral and written communications. Accountable for the maintenance of the research laboratory and greenhouse, ensuring a very safe and productive working environment. To supervise and train lab technicians and interns in laboratory operation procedures and the operation of equipment in the laboratory. Any other seed biology and technology development duties as may be reasonably required by the company, QA Manager or Physiology Manager. The individual will work primarily in a laboratory environment, with some greenhouse and field work. REQUIRED KNOWLEDGE/SKILLS/ABILITIES: Minimum five years research experience in seed science and technology. Proved track record in developing practical solutions in horticulture or seed technology. Competences and experience in seed quality, testing, storage behavior, dormancy/germination preferred. Competences in experiment design, data analysis and image processing. Experience in hands on cell biology and molecular biology experience. Must have a creative mindset and a pragmatic attitude. Must be able to perform job activities accurately and efficiently. Attention to detail. Must be comfortable working in an agricultural environment. i.e. with agricultural chemicals and in environments where temperatures may be hot or cold. Must have good communication skills. Must be agile to changing work demands, techniques, or approaches and must have the ability to adapt quickly to such circumstances. EDUCATION REQUIREMENTS: Master or PhD degree in plant biology, horticulture or agronomy, with emphasis on vegetable physiology or seed science. EXPERIENCE AND BACKGROUND: Computer literacy and data analysis skills. Good verbal and oral communication skills in English. Minimum five years' research experience in vegetable or seed science in the industry or public sector. WORKING CONDITIONS/PHYSICAL DEMANDS: Must be able to work in a greenhouse environment, under hot and cold temperatures for several hours at a time (15%). Must be willing to work with chemicals and pesticides, and other potentially irritating substances, such as fertilizers and plant growth regulators. Must be able to wear personal protective equipment when necessary and/or required to apply pesticides. Must be able to work in dusty conditions and willing to work alone and without direct supervision for extended periods. Must be able to stand for long periods of time. Must be available to work overtime, weekends and/or holidays when the workflow demands. COMPENSATION & BENEFITS: Salary: $80,000-$84,000 per year Medical, Dental & Vision Insurance coverage for employees and their families Basic Life & AD&D Insurance 401k program with company match Profit Sharing program (via 401k) Holiday & Performance Incentive Bonus program Paid Vacation: 10 days per year to start, increases with tenure Sick Leave: 1 hour accrued per 30 hours worked for first 30 days, 6.67 hours per month after. 14 paid company holidays, 2 floating holidays & birthday off Paid Family Leave: 15 days after 12 months of service for FMLA qualifying events * To perform this job successfully, an individual must be able to perform each essential duty (as described above) satisfactorily. Reasonable accommodations may be made to enable Individuals with disabilities to perform these essential functions.

Job DescriptionDescriptionAlign Technology is the industry leader and innovator in medical devices which focuses on revolutionizing the digital dental and orthodontic industry. Align Technology is looking for an R&D Engineer III, Core Product for our San Jose, CA office. This exciting new role would be part of a culture that is helping to improve lives every day through digital dentistry. The R&D Engineer III, Core Product candidate should have exceptional skills with product research and development in the medical device industry. The R&D Engineer III, Core Product will be the lead engineer responsible for planning, leading, and executing projects focusing on product design and design improvement. They will work closely with internal and external resources in a multidisciplinary team working with materials, software, and manufacturing to conduct research and development in the areas of product performance, design, and improvement. This role will be part of Align Technology's goal to deliver our clear aligners (Invisalign ) to our customers. Role expectations Lead product development projects and research projects until product launch Work independently to develop and evaluate new products and solutions and adapt and improve existing ones Design and evaluate product prototypes with biomechanical test models and experimentation Design, build, and verify test hardware, software, and systems as needed Define and conduct procedures for bench top testing to evaluate product performance, including efficacy, reliability, verification, and validation Work with clinical team to conduct pilot studies and other investigations Simulate real world conditions and measure outputs using sensors Collaborate with diverse, cross-functional teams to incorporate design and features into prototypes Understand and master complex systems with sound mechanical principles Define procedures to evaluate product performance and conduct bench top testing Responsible for ensuring that testing covers efficacy, reliability, verification, and validation Perform statistical data analysis and interpretation Perform and document work in accordance with FDA/ISO regulations, including test protocols, test results, and other requirements Collaborate with manager and cross-functional team in creating product and test plans Communicate with professionals in the field at all levels and transition information into product improvement Conceive new product and technology development plans Work in a fast-paced environment and meet critical deadlines Problem-solve issues with attention to detail Provide general engineering support in R&D What we're looking for B.S, M.S., or Ph.D. in Mechanical/Biomedical Engineering or other related degrees/equivalent work experience. 5+ years of experience in biomedical research and/or product development Theoretical and experimental background in structural mechanics and/or biomechanics Experience with additive manufacturing and rapid prototyping processes for product design and development Experience with 3D modeling using CAD software, Solidworks preferred Experience with scripting/programming Experience with finite element analysis Experience in medical device industry Experience in orthodontics and/or dental industry Pay TransparencyIf provided, base salary or wage rate ranges are the range in which Align reasonably expects to set a candidate's pay for the posted position. Actual placement depends on the individual skills and experience level of a candidate plus the total compensation and equity across team members. For other locations outside of the primary location, the base salary range will be adjusted geographically. For Field Sales roles, the salary listed is the base pay only and does not include the applicable incentive compensation plan. A cost of living adjustment may be added to base pay for higher cost areas in the U.S. Our internship hourly rates are a standard pay determined based on the position and your location, year in school, degree, and experience.