Research and development technician jobs in Eastvale, CA - 397 jobs

About the Company HEYTEA is a pioneering and trend-setting new-style tea drink brand born in 2012. We are obsessed with creating inspired drinks and bakery items that surprise and delight our customers worldwide. Through continuous innovation with premium ingredients, we redefine the tea-drinking experience. Now, as we expand our footprint in the United States, we are looking for a passionate Bakery R&D Specialist to join our journey and craft the next signature bite that resonates with the American palate. About the Role As a Bakery R&D Specialist, you will be the culinary architect behind HEYTEA's bakery lineup in the U.S. market. You will bridge Eastern inspiration with Western tastes, developing innovative, high-quality baked goods that complement our iconic tea drinks. This role requires a unique blend of technical expertise, creative flair, and cross-cultural communication skills. Responsibilities Product Development & Innovation: Lead the end-to-end development of new bakery items (e.g., bread, cake, pastry) for the U.S. market, from conceptualization to launch. Adapt and reinvent HEYTEA's classic bakery items to suit local ingredient availability and consumer preferences. Conduct thorough market research and trend analysis to capture the latest food movements. Technical Execution & Quality Control: Formulate recipes, specify ingredients, establish precise SOPs, and set quality standards. Collaborate with supply chain and production teams for sourcing and pilot production. Cross-functional & Cross-cultural Collaboration: Serve as the key liaison between the U.S. team and HEYTEA's Global R&D Center in Shenzhen. Communicate project progress, challenges, and insights effectively in both Chinese and English. Work closely with marketing, operations, and training teams to ensure successful product launches. Qualifications Bachelor's degree or higher in Food Science, Culinary Arts, Bakery Science, or a related field. 3+ years of hands-on experience in bakery R&D, preferably within the premium café, chain restaurant, or retail food industry. Proficiency in both written and spoken Chinese (Mandarin) and English is essential for daily business communication. Deep understanding of American consumer tastes and the local bakery ingredient landscape. Strong creative and problem-solving skills, with a passion for innovation. Ability to thrive in a fast-paced, dynamic, and cross-cultural team environment. Required Skills Technical expertise in bakery product development. Creative flair for innovative baking. Cross-cultural communication skills. Preferred Skills Experience in premium café or retail food industry. Knowledge of local ingredient sourcing. Pay range and compensation package Competitive compensation and benefits package. Equal Opportunity Statement HEYTEA is committed to diversity and inclusivity in the workplace. We encourage applications from individuals of all backgrounds and experiences. 关于公司 HEYTEA是一个开创性和引领潮流的新式茶饮品牌,成立于2012年。我们专注于创造灵感饮品和烘焙产品,给全球客户带来惊喜和愉悦。通过持续创新和优质原料,我们重新定义了饮茶体验。现在,随着我们在美国市场的扩展,我们正在寻找一位充满热情的烘焙研发专员加入我们的旅程,打造能触动美国味蕾的下一款经典产品。 关于职位 作为烘焙研发专员,您将成为喜茶美国市场烘焙产品线的“美食建筑师”。您将连接东方灵感与西方口味,研发创新,高品质的烘焙产品,以搭配我们标志性的茶饮。此职位需要卓越的技术专长,创造力和跨文化沟通能力。 职责 产品研发与创新：主导针对美国市场的新烘焙产品（如面包,蛋糕,点心）从概念到上市的全流程研发。 调整并重塑喜茶经典烘焙产品,以适应本地原料供应和消费者偏好。 进行深入的市场调研和趋势分析,捕捉最新饮食潮流。 技术执行与质量控制：设计配方,指定原料,建立精准标准作业程序,设定质量标准。 与供应链及生产团队协作,完成原料寻源和试生产。 跨职能与跨文化协作：作为美国团队与喜茶全球研发中心（深圳）的关键联络人。 熟练运用中英文双语,有效沟通项目进展,挑战与洞察。 与市场,运营及培训团队紧密合作,确保产品成功上市。 任职要求 食品科学,烹饪艺术,烘焙科学或相关专业本科及以上学历。 3年以上烘焙研发实践经验,优先考虑具有高端咖啡厅,连锁餐饮或零售食品行业背景者。 必须具备流利的商务中文（普通话）和英文书面及口语沟通能力。 深刻理解美国消费者口味及本地烘焙原料市场。 出色的创造力和解决问题能力,对创新充满热情。 能够适应快节奏,动态变化的跨文化团队环境。 我们提供 参与构建喜茶美国烘焙产品线,发挥关键影响力的机会。 在全球创新品牌中工作,与行业顶尖人才协作。 具有竞争力的薪酬福利体系。 通过深入全球研发体系,获得独特的个人与职业成长机遇。

Join a pioneering startup founded by a renowned Professor, in shaping the future of environmental sustainability. As a Senior R&D Scientist, you will lead the charge in developing cutting-edge CO2 capture technologies, driving innovations that can significantly impact the global fight against climate change. Why You Should Apply Be a key player in pioneering CO2 capture technology. Competitive salary and benefits package. Work with a team of distinguished scientists and engineers. Contribute to groundbreaking research with global environmental impact. Join a startup environment that values diversity, collaboration, and innovation. What You'll Be Doing: Collaborate with the head of Product Engineering to scale up MOF/COF-based CO2 capture systems. Model the kinetics, thermal transfer, and CO2 adsorption/desorption mechanisms. Develop and optimize models for CO2 capture, including energy efficiency and air flow. Design and scale technologies from prototype to commercial stage. Optimize system parameters to enhance performance and efficiency. Collaborate with R&D scientists on technical specifications. Evaluate and manage sourcing of materials and components. Establish QC/QA processes and maintain detailed electronic notebooks. Contribute to the company's intellectual property and participate in technical meetings. About You: PhD in mechanical engineering, chemical engineering, or a related field with a strong research background. Experience in CO2 capture industry and pressure swing adsorption systems. Proficient in thermodynamics, fluid mechanics, and heat transfer. Over 5 years of industrial R&D experience, with 3-5 years in the CO2 field. Skilled in designing system-level prototypes and using simulation tools. Familiar with health and safety procedures in production. Excellent teamwork, problem-solving, and communication skills. How To Apply We'd love to see your resume, but we don't need it to have a conversation. Send us an email to *********************** and tell us why you're interested. Or, feel free to email your resume. Please include Job#19656

Project Chemistry is dedicated to transforming the beauty industry with innovative and advanced biotech-driven formulations. We strive to redefine possibilities in science to offer advanced end-to-end solutions. Our mission is to empower emerging and established beauty brands with groundbreaking products that set new standards and define the future of beauty. By bridging technology and creativity, we aim to lead the way in beauty innovation. If you love experimenting in the lab, exploring new technologies, and pushing formulation boundaries, you'll feel right at home here. Role Description We're looking for a curious, creative, and hands-on R&D Formulation Chemist who's excited to explore new ingredients, technologies, and ideas. This is a full-time, on-site role for a Lead R&D Formulation Chemist, located in Irvine, CA. The role involves leading research and development efforts, formulating innovative cosmetic products, conducting laboratory experiments, optimizing product performance, and ensuring compliance with regulatory standards. The lead chemist will also collaborate with cross-functional teams, mentor junior staff, and drive high-quality standards throughout all project phases. Key Responsibilities Formulate and batch cosmetic products across multiple categories Develop stable, high-performance formulas balancing efficacy, sensorials, cost, and regulatory requirements Lead solubility mapping and incorporation of novel or challenging actives Support scale-up and technology transfer with contract manufacturers Oversee lab operations, equipment, and SOPs; mentor junior staff Present formulation strategies and scientific rationale to clients Stay current on clean beauty standards and global regulatory requirements Qualifications BS or MS in Chemistry, Chemical Engineering, or related field 7+ years of hands-on cosmetic formulation experience Strong knowledge of raw materials, technologies, and delivery systems Experience with scale-up, manufacturing troubleshooting, and tech transfer Excellent communication skills and comfort in client-facing settings Authorized to work in the U.S. Why Join Us? At Project Chemistry, you'll have the opportunity to work on cutting-edge innovation, influence IP-driven development, and play a key role in shaping next-generation beauty products-all within a collaborative, entrepreneurial environment.

A top management consulting firm based in California seeks a Research Leader to manage a multi-themed research program. The successful candidate will engage with senior leadership teams to advise on technology strategies and deliver an annual research agenda. Candidates should have an MBA and 8-16 years of experience in research or consulting, alongside strong communication and analytical skills. This position offers international exposure and a dynamic work environment. #J-18808-Ljbffr

The ideal candidate is expected to demonstrate current knowledge and understanding of regulatory requirements and practices (GMP, USP, ICH guidelines). Familiar with analytical techniques such as HPLC/UPLC with various detectors (CAD, RI, UV/PDA, etc.), GC-FID, particle size distribution, physical appearance assessments, pH meter, turbidimeter, osmometer, viscosity measurements, rheometry for ophthalmic drug products and/or drug substances. Responsibilities: Collaborate with the team to design, plan, and perform independently variety of project-oriented analytical assignments (method feasibility, qualification, development stability, Ad-Hoc studies) in a timely and efficient manner. Maintain accurate documentation of experiments and results/analytical findings in electronic lab notebook. Additional responsibilities include proper maintenance of laboratory equipment and instrumentation to ensure laboratory operational capability and procurement of necessary chemical reagents, reference standards, and other components from appropriate sources. Independently complies, evaluates, and/or statistically analyzes technical data. Core Values: Candidates are energetic, proactive, collaborative and have cross-functional communication skills, and are willing to work with various team members/groups and learn new techniques. Participate, collaborate, and contribute at group and projects meetings as required by presenting and discussing data and designing follow-up experiments. A working knowledge of phase-appropriate analytical development (method feasibility, validation, and stability programs) is preferred. The candidate must conduct their work activities in compliance with all company internal requirements and with applicable regulatory requirements. Company internal requirements include compliance with ethics, environmental health and safety, financial, human resources and general business policies, requirements, and objectives. Skills: Strong technical writing and communication. Must be proficient using Word, Excel, and statistical programs for analytical data evaluation. Ability to review and understand new and innovative analytical methods and provide critical feedback. Education and experience: M.S. in Analytical Chemistry or related discipline with minimum 2 years of experience or B.S. in Analytical Chemistry or related discipline with minimum 3-5 years of experience in analysis of pharmaceutical products or pharmaceutical method development and validation with strong report writing, documentation and organization skills. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. 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. Recruiter Details: Name: Shivangi Shivpuri Email: ********************************* Internal Id: 26-00892

What We Do / Project The Senior Design Researcher will champion user-centered research and design practices for internal, web-based applications and platforms used by business stakeholders. This role focuses on uncovering user needs, synthesizing insights, and guiding the design of intuitive, data-driven experiences that simplify complex workflows and enable faster, more informed decision-making. Job Responsibilities / Typical Day Strategy & Leadership Define and drive a clear research vision aligned with product and business goals Prioritize research initiatives to maximize impact and inform product strategy Foster a research-driven culture by promoting best practices and deep understanding of user needs Mentor and coach team members to strengthen research capabilities and elevate overall impact Research Planning & Execution Plan and conduct user interviews, workshops, and usability testing to uncover explicit and latent user pain points Partner closely with UX Designers, Technical Product Owners, and Business Analysts to execute research initiatives Apply appropriate qualitative and quantitative methods to inform design decisions Analysis & Communication Synthesize research findings into actionable insights Create impactful research artifacts such as personas, archetypes, user journey maps, and experience maps Present findings clearly and persuasively to diverse stakeholder groups Collaborate with design teams to translate complex business rules and data into intuitive, user-friendly solutions Facilitation, Collaboration & Advocacy Advocate for end users throughout the design and development lifecycle Collaborate with cross-functional teams, including UX, product, engineering, and delivery teams, to ensure insights are incorporated into designs, user stories, and final solutions Support iterative product development through ongoing research and validation Must-Have Skills / Requirements User Research Expertise: 8+ years of experience conducting user interviews and eliciting pain points and requirements Quantitative Research & Measurement: 8+ years of experience analyzing user behavior data to inform system and product design Mentorship & Coaching: 5+ years of experience mentoring team members and promoting user-centric thinking Nice-to-Have / Preferred Qualifications Design Thinking certification Experience designing enterprise-level products or internal tools Background in software design and development Experience in media and entertainment environments Familiarity with sales planning and execution workflows Branding experience Soft Skills & Core Competencies Deep theoretical and practical knowledge of qualitative and quantitative research methodologies Experience working on moderate to highly complex projects Strong portfolio demonstrating research process and impact, including: Research roadmaps Personas / archetypes User journey maps Experience maps Mental model diagrams Research reports and presentations Excellent written, verbal, and presentation skills Strong ability to empathize with users and uncover motivations Proven ability to mentor and collaborate across disciplines Experience working in agile, cross-functional teams Ability to work independently with minimal supervision Comfortable in fast-paced, evolving environments and resilient in the face of change Technology Requirements Prototyping tools: Figma or Adobe Creative Suite Survey tools: M365 Forms, SurveyMonkey Collaboration tools: Miro Documentation and reporting tools: Jira, Confluence, M365 Education Bachelor's degree in Design, Human-Computer Interaction (HCI), Sociology, Psychology, or a related field

HPLC Chemist Kelly Science & Clinical is seeking an HPLC Chemist for a temp-to-hire position at a cutting-edge client in Carson, CA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Pay: $24 - $25/hr Schedule: 1st shift, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends, and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Overview This client is an industry-leading company that's leading the way in high-quality analytical testing services. As an HPLC Chemist, you will be performing instrumental analysis using HPLC Isocratic/Binary systems, operating, troubleshooting, process validation, and method development of the HPLC system. You will also be responsible for preventive maintenance, calibration, and generating IQ, PQ, and OQ documentation for new equipment. Responsibilities: Perform preventive maintenance of instruments and equipment. Follow SOP, Safety, and GMP guidelines. Conduct monthly, weekly, and daily lab equipment calibration. Generate IQ, PQ, and OQ documentation for new equipment. Determine daily system suitability. Prepare sample solutions, standards, and reagents. Prepare lab batches at various concentrations for method validation. Conduct placebo batch validation and testing of new product formulas. Troubleshoot and maintain the HPLC system daily. Update and maintain the system database. Maintain accurate laboratory notebooks for traceability. Dispose of solvent waste following safety protocols and procedures. Approve and release internal assay results. Investigate and report Out-of-Spec (OOS) results to the appropriate department. Maintain supply inventory. Develop and validate new methods for new product assays. Prepare HPLC documentation for audits. Provide training and support for all new incoming employees. Supervise HPLC Lab Technicians. Qualifications: BS in chemistry or any science-related field. Experience in an HPLC lab setting. Proficient in Microsoft Word, Excel, and PowerPoint. Hands-on experience with HPLC Isocratic/Binary instrumental analysis. Strong troubleshooting, process validation, and method development skills. Knowledge of GMP compliance and laboratory safety protocols. What happens next: Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

Company Size: 250/ Team Size: 15 Industry: Manufacturing Duties & Responsibilities Perform preventive maintenance of instruments or equipment. Follow SOP, Safety and GMP Monthly, weekly, and daily lab equipment calibration. Generate IQ PQ OQ for new equipment. Determine daily system suitability. Preparation of sample solution, standards, and reagents Preparation of lab batches at various concentrations for method validation. Conduct placebo batch and perform of validation on new product formula. Daily maintenance and troubleshooting when the system error. Update/Maintain System Database. Maintain accurate laboratory notebook for traceability. Disposal of solvent waste follow safety protocols and procedures. Approve and release internal assay results Investigate & Report OOS to appropriated HPLC Department. Maintain supply inventory. Requirements Degree in chemistry and any science-related field or work experience in HPLC Lab setting. Instrumental analysis using HPLC. Operating, troubleshooting, process validation, and development of the HPLC system. Proficient in Microsoft Word, Excel, and PowerPoint. Pay: $25/hr.

Job Description A leading company in the cosmetics and chemical industry is seeking an experienced R&D Research Scientist to join its team. This role involves product formulation, ingredient research, and regulatory compliance to support the development and enhancement of cosmetics and chemical products. If you have a strong background in product development and formulation, this is a great opportunity to advance your career. Requirements Key Responsibilities: Develop and improve formulations for cosmetics and chemical-based products. Conduct research on raw materials, active ingredients, and product stability. Ensure compliance with cosmetic regulations and safety assessments. Collaborate with internal teams to enhance product performance and innovation. Optimize product textures, stability, and functionality through ingredient research and testing. Qualifications: Degree in Chemistry, Chemical Engineering, or a related field. Experience in cosmetics or chemical product development. Strong understanding of formulation design and ingredient interactions. Knowledge of cosmetic industry regulations and safety assessments. Ability to conduct raw material analysis and apply innovative research to product development. Benefits Benefits: Comprehensive Health Insurance Paid Time Off (PTO) 401(k) Retirement Plan Performance-Based Employee Awards Reimbursement for Business-Related Expenses Complimentary Breakfast & Lunch Provided If you are passionate about cosmetic and chemical innovation and eager to contribute to a cutting-edge R&D team, apply today.

The R&D (Packing) Specialist position encompasses a critical support role by managing and executing the product development and production activities. This area of responsibility are required to successfully produce R&D package product samples for both internal and external customers. Essential Duties and Responsibilities The described are considered essential to the job and representative of those that must be met by an employee to successfully perform the essential functions. Qualified individuals must have the ability with or without reasonable accommodation to perform the following functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Under R&D Manager's supervision: Understand variety of cuisines and be able to explain, analyze and formulate soup, in both creative and traditional fashion. Benchmark with other companies' products. Perform activities relevant to the product development process, which may include but not limited to conceptualization, formulation and prototype evaluation, optimization and standardization, cost calculation, commercial translation and product launch. Select new materials and negotiate prices for new materials and current materials, updating material list or vendors as needed with the goal of reducing the cost of the current materials. Design and test products to ensure shelf-life stability and all aspects of product (flavor, color and texture, nutritional content etc.). Conduct variety of applicable tests and analyses on products to determine inherent properties and present analysis of results to the department for further product development and improvement. Research consumer awareness or trends, relating to product development (including legal issues). Execution of research on consumer taste preference through validation internally and/or externally. Collaborate with process engineers, plant management, marketing specialists and external customers in order insure projects remain on schedule and within budget. Conduct production trials to ensure successful launch of new and revised products. Monitor production to confirm plant capability and conformance to design criteria and train plant operation. Understand general requirements of laws and regulations related to but not limited to food labeling and food additives. Report and present oral and written updates including product demonstrations to team and customers. Prepare all necessary document such as, but not limited to, test report, Standard Formulation, Standard Process, any other necessary standard/process in commercialization and ensuring food safety. Manage materials (including the purchase and shipping of lab apparatus) and supply inventory. Other job duties as assigned. Supervisory Responsibilities: This job has no supervisory responsibilities. Qualifications and Requirements Required Qualifications: Bachelor's degree (B.S.) or equivalent combination of education and experience. B.S. degree in nutrition, food science, or food technology is preferred. 2+ year related experience in Research and Development or related field in the food industry. #LI-hybrid About Us It started with the inspiration of the creator of instant noodles, founder Momofuku Ando, in 1958. Since we entered the U.S. in 1970, our flagship brands, Cup Noodles, and Top Ramen have maintained a firm foothold in U.S. pop culture. We invite you to join Team Nissin to support this legacy of innovation and to deliver noodle happiness to consumers, employees, partners, and the community in a meaningful and sustainable way. Let's evolve how people think about instant ramen as you discover opportunities for professional growth while being part of this $4 billion global company built from a simple block of noodles. Nissin Foods (USA) Co., Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, or sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. As a federal contractor, Nissin Foods participates in the federal government's E-Verify program, which confirms employment authorization of all newly hired employees through an electronic database maintained by the Social Security Administration and Department of Homeland Security. The E-Verify process may be completed in conjunction with the Form I-9 Employment Eligibility Verification to check the work authorization status of persons who have been offered employment at Nissin Foods. E-Verify is not used as a tool to pre-screen candidates. For up-to-date information on E-Verify, go to ************** If you are a qualified individual with a disability or a disabled veteran, you have the right to request an accommodation if you are unable or limited in your ability to use or access our career center as a result of your disability. To request accommodation, contact Nissin Foods (USA) Co., Inc. Human Resources.

The Production Scientist is responsible for a upscaling R&D small scale work into GMP large scale manufacturing, Oversee production activities of the assigned projects, collect and analyze GMP data, Author and review quality documents such as MBPR, R.A, PPQ protocol, drive yield and process improvement projects, update the customer with the GMP activities, ensuring production processes meet quality standards, or maintaining equipment efficiency. This role contributes directly to PolyPeptide's commitment to delivering exceptional quality and on-time delivery to our customers Key Responsibilities: * Review and approve quality and validation documents as the production representative that does not need managers approval (MBPR, CC, SOP, PQE, PPQ related documents, educational certificates etc.) * Perform Operational assessments. * Prepare weekly slide deck presentations on project updates to internal and external stakeholders. * Lead and/or prepare and/or support product investigations using root cause analysis techniques (interviewing, fishbone diagram, 5 whys etc) and summarizing findings in written reports and oral presentations to internal and external stakeholders (QIRM, OOT, OOS, RCI, CAPA/Task) * Author, prepare and support Deviations, process change controls, CAPA during project execution. * Prepare Change Control Change Request and list of change document as part of MBPR generation (CC general and for MBPR) * Draft and review Standard Operating Procedures (QUMAS) * Conduct Risk Assessment (CRIA, RIA, FMEA) * Approve quality documents as the production representative that does not need managers approval (MBPR, ARM, CR, SOP, PQE, validation documents, educational certificates etc.) * Generate detailed Gannt chart of batch schedule. * BOM generation and Process mapping (soon to include route & formula) * Provide on-floor and remote 24/7 technical support to Production during project execution (including weekends, grave, and night shifts), e.g. make go/no go decisions on IPC-results regarding process steps or troubleshooting issues. * Project management of operation activities related to batch preparation/ execution (equipment/ IPC validation, hold time study, etc…) * Draft, format and improve MBPR template. * Support technology transfer activities (generation of comparability report, identification of CPPs, review and approve validation PPQ documents, generation of BPR etc). * Author and review campaign reports. * Raw material OOS assessment * Conduct Bottle neck analysis and Gap analysis of unit operations. * Prepare Process capability analysis. * Conduct cost analysis and forecasting. * Liaise with cross functional groups (Production, QA, QC, Development, Project Management, Sale, Regulatory, Supply Chain etc.) to support the planning and execution of manufacturing operations. * Collaborate with PD to Design small scale experiments to support investigations or process improvement initiatives. * Lead, mentor and train Operators and team members as part of upstream and downstream process knowledge transfer on MBPR and unit operations. * Support continuous improvement initiatives. * Manually Collect, trend, and analyze in process data as part of process monitoring to determine yields and change points. * Support QA and regulatory with responding to comments by clients on executed BPR and NDA/BLA, submission. * Support Validation activities during the planning execution of PPQ runs (prepare supporting PPQ document, e.g. equipment calibration and suitability, analytical methods, hold time study, PPQ strategy etc). * Support regulatory review of documents. * Process Mapping * Routes and Formula on AX to be added to our responsibilities. Qualifications: Education & Experience * Required Education: * Advanced degree in chemistry, Biochemistry, Engineering, or a related field. * Formal training or coursework in GMP, pharmaceutical manufacturing, or related regulatory standards is highly desirable. * Relevant industry certifications (e.g., Lean Six Sigma, GMP compliance) are a plus. * Experience: * Minimum 5 years in pharmaceutical manufacturing GMP production or MS&T team, peptide manufacturing experience preferred. * Proven ability to independently operate and troubleshoot production equipment and execute complex manufacturing procedures. * Demonstrated success in working autonomously while managing multiple production tasks and priorities. Skills & Competencies * Technical Skills: Basic understanding about SPPS GMP manufacturing, Proficiency in HPLC systems, cGMP processes, Data analysis (Minitab experience is preferred). * Soft Skills: Strong problem-solving, collaboration, Microsoft Data analysis (Minitab experience is preferred), Technical writing, and communication skills, and Microsoft office. * Competencies: * Strategic Scientific Judgment * Quality and Regulatory Leadership * Complex Problem Solving and Decision Making * Technical Influence and Innovation * Cross-Functional Leadership and Collaboration Salary: $115K-$130K We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Under minimal supervision of the Principal Investigator, the Lab Research Technician will work independently to: * Design and perform biochemistry and molecular biology experiments including protein expression and purification, transformations, plasmid preparations, gel electrophoresis, and binding assays, and analyze binding data on Prism. * Write and modify laboratory Standard Operating Procedures (SOPs) as needed. * Understand and adhere to laboratory safety guidelines. * Keep organized records of experiments and results through the use of a lab notebook and standard word processing programs (Word, Excel, PowerPoint)

. The SUD Counselor I must be registered as a Substance Abuse Counselor from an approved/accredited California agency with preferably a minimum of two years' experience in the human service field and demonstrated expertise in substance abuse treatment, relapse prevention, and recovery. As per contract, all staff hired MUST be fully vaccinated against COVID-19 and when eligible, receive their booster shot. Prototypes, a program of HealthRIGHT 360's residential substance use disorder (SUD) program is a new program contracted with Department of Public Health's (DPH) Substance Abuse Prevention and Control (SAPC) program for residential drug Medi-Cal (DMC) services for up to 99 adult men and women: 33 that are for men who are judicially involved, 33 for men, and 33 for women. The BHC's residential DMC program will employ 100 people and works closely with the other BHC programs to provide a continuum of services for low income/Medi-Cal population. The program is located on the campus of Martin Luther King Jr. Hospital in the Willowbrook area of South Los Angeles and will serve all LA County residents. The SUD Counselor I (Floor Staff/Food Tech) is a registered substance use disorder professional who maintains registration from an approved/accredited California agency. The SUD Counselor I works in collaboration with other members of the multidisciplinary team to ensure best possible treatment outcome for the client and provide treatment in accordance with HealthRIGHT 360's philosophy, goals, policies, mission and vision. The SUD Counselor I provides supervision and oversite of the clients throughout the facility with shifts ranging to provide 24/7 coverage. SUD Counselor I provides facility coverage by supervising the clients during chores, visiting hours, meal times, medication line, detox, donations, groups, and free time. The SUD Counselor I is customer service focused and frequently provides crisis intervention and client stabilization. The SUD Counselor I has a high degree of self-awareness and the ability to stay calm under pressure. Key Responsibilities Knowledge Required: Knowledge issues of related to substance abuse, mental health, and criminal background. Culturally competent and able to work with a diverse population. Strong proficiency with Microsoft Office applications, specifically Word Outlook and internet applications. Skills and Abilities Required: Professionalism, punctuality, flexibility and reliability are imperative -Strong computer skills, including Outlook, Excel, Word and PowerPoint. Excellent verbal, written, and interpersonal skills -Integrity to handle sensitive information in a confidential manner. Action oriented. Strong problem-solving skills. Excellent organization skills and ability to multitask and juggle multiple priorities. Outstanding ability to follow-through with tasks. Ability to work cooperatively and effectively as part of interdisciplinary team and independently assume responsibility. Strong initiative and enthusiasm and willingness to pitch in whenever needed. Able to communicate well at all levels of the organization including working with organization leadership and high-level representatives of partner organizations. Able to work within a frequently changing project scope while maintaining overall direction and structured priorities. Education and Knowledge, Skills and Abilities Education Requirements: Registration as Substance Abuse Counselor from an approved/accredited California agency. Experience: Preferably a minimum of two years' experience in the human service field and demonstrated expertise in substance abuse treatment, relapse prevention, and recovery. Experience working with clients experiencing acute withdrawal from substances. Knowledge of and experience with providing trauma informed services. Experience delivering evidence-based practices. In compliance with the California Department of Public Health's mandate, all employees must be able to provide proof of COVID-19 vaccination. Medical and religious exemptions are available. Tag: IND100.

Build complex prototypes from verbal instructions and/or simple drawings and perform testing and documentation duties with moderate supervision. Job duties: + Fabricate complex prototypes, manufacturing processes, and fixtures. + Set up and conduct tests of completed units or components under operational conditions to investigate designs or to obtain data for development and standardization. + Record and analyze test procedures and results, numerical, and graphical data. + Support production or process development as required. + Set up, adjust, and operate laboratory equipment and instruments such as microscopes. + Provide input into product design, processes, and testing. + Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. + Perform additional duties as assigned. **Salary Range** $27.82/hr - $36.52/hr Financial compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. **Auto req ID:** 13162BR **Location MV:** Aliso Viejo, California, USA **Department Name:** 800-California Interventional Systems (CAIS) **Qualifications:** 1. High school diploma or equivalent. 2. A minimum of five (5) years of related work experience. 3. Good written and verbal communication skills. 4. Ability to read, write, and speak in English. 5. Strong computer skills including MS Word, Excel, Teams, Outlook, etc. 6. Ability to read and understand technical documentation. 7. Good laboratory or manufacturing practices and ability to follow required safety procedures. 8. Basic math skills. **Desired Qualifications** 1. Experience in the medical device industry. 2. Working knowledge of CAD software platforms like SolidWorks. 3. Knowledge of materials and suppliers. 4. Knowledge of processes and/or machinery and equipment used in the development and production of medical devices. **EEO** We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law. **Fair Chance Ordinance** If you are applying to perform work for Terumo Neuro in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Terumo Neuro reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Terumo Neuro will consider for employment qualified job applicants with arrest or conviction records in accordance with the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance. **External-Facing Title:** Sr. Technician, R&D **Salary Range:** $27.82/hr - $36.52/hr Financial compensation packages may be higher/lower than what is listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.

Job Description Do you want to build a stronger, more sustainable future and cultivate your career? Become a part of the Dermalogica Research and Development team. We are looking for a talented Chemist to be based at the Corporate Headquarters in Carson working on-site with the R&D department in a temporary capacity. Role Overview Seeking a temporary R&D Chemist to support bench scale formulation, batching, and stability placement for skincare products. This is a hands-on, execution focused role supporting active development programs in the lab. Key Responsibilities Prepare bench scale batches following established formulas and SOPs Support stability setup including labeling, documentation, and sample placement Accurately record batch data, observations, and deviations Maintain lab organization, raw material handling, and equipment cleanliness Partner with formulation and stability teams to support active projects Required Skills & Experience BS in Chemistry, Cosmetic Science, Chemical Engineering, or related field 1-3 years hands on formulation or lab experience (cosmetics or personal care preferred) Strong bench skills including weighing, mixing, heating/cooling, and pH adjustment Familiarity with stability programs and sample tracking Detail-oriented with strong documentation and organizational skills Able to work independently with clear direction Proficient in Microsoft Office (Excel, Word, Outlook) for documentation and data entry The position is based at the corporate headquarters in Carson, CA, and will be fully on-site, 5 days per week (no remote or hybrid). The pay rate for this role is $35 per hour. Ready to make a meaningful impact and advance your career with a global brand revolutionizing the skincare industry? Apply now and complete your online application. All applications will be reviewed, and our HR team will contact you if your skills align with the position. Dermalogica is an equal opportunity employer committed to fostering an inclusive culture where all employees are valued, supported, and empowered to succeed.

The R&D Chemist II/III within the Process Development Group will be responsible for purification, analysis, and isolation of GMP grade peptides under GMP regulations. This work will encompass preparative and analytical chromatography, and lyophilization. What you will do * Perform preparative and analytical reversed-phase high performance liquid chromatography (HPLC) and isolation operations with direction from supervisor * Follow written procedures such as Standard Operating Procedures (SOP) and Batch Production Records (BPR) * Comply with SOP's in all aspects of the work and follow GMP regulations * With appropriate training, become well-versed in operation of specific chromatography platforms used in the GMP Manufacturing Group * Document accurately purification conditions and yields in the Batch Production Records (BPR) * Work in close cooperation with synthetic chemists to meet project commitments with regard to deliverable timelines, quantity, and quality * Constantly monitor and improve practices by learning from past projects * Ensure that all laboratory safety and housekeeping standards are met Qualifications * Bachelor's degree in chemistry, biochemistry, or bioengineering with a minimum 3 years' experience or * Master's degree with 1+ year of experience * Hands-on experience in preparative and analytical reversed-phase high performance liquid chromatography (HPLC) and isolation operations in a GMP environment * Hands-on laboratory experience (academic acceptable, industry preferred) in protein or peptide chemistry * Experience in RP-HPLC and ion exchange chromatography * Experience with synthesis and/or purification * Strong knowledge of GMP regulations and ICH guidelines * Good laboratory notebook and data organization skills * Excellent written and oral communication skills * Basic computer knowledge, including Microsoft Word, Excel and PowerPoint * Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment * Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues * Detail oriented with the ability to troubleshoot and resolve problems * Ability to work independently and manage one's time * Communicate effectively and ability to function well in a team environment Base Hourly Range: * Chemist II: $30.49 - $41.93 * Chemist III: $38.61 - $53.09 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees' environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. Please note: unsolicited resumes from recruitment agencies will not be considered. Share this job posting by email

ROLE DESCRIPTION Job Title: Research and Development Chemist Department: Research and Development Reports To: Research and Development Manager FLSA Status: Exempt/Full-Time Basic Purpose Formulate personal care, skincare and haircare products for customers in contract manufacturing environment via innovation, tech transfer, or reverse engineering. Essential Duties and Responsibilities Develop formulas using customer beliefs and direction by understanding the balance between cost, claims, and functionality. Contribute to customer marketing goals and company growth goals through innovation. Project management of priorities and deadlines to ensure customer requirements are met. Act as “eyes of customer” for all pilots, launches, and approvals. Work collaboratively with cross functional teams, effectively meeting deadlines. Perform pre-production R&D laboratory tests to optimize scale-up process and highlight critical parameters affecting production. Manage handoff from R&D to compounding including collaborating on manufacturing process development, batch records, and tank selection. Follow all GMP guidelines, SOP's, and safety requirements. Track and monitor stability of prepared samples. Identify and resolve process deviations and non-conformances and provide corrective actions to eliminate future discrepancies. Keep current on chemistry trends in ingredients, products, and technology. Skills/Knowledge/Abilities Bachelor's degree in Chemistry, Biology, Engineering, or related field or equivalent experience. At least 2 years of experience formulating for personal care, skin care, and/or haircare. Working knowledge of Topical cosmetic and OTC manufacturing and R&D operations. Strong project management skills and ability to work independently. Demonstrated capability to drive improvement, efficiency, and cost savings. Experience with cGMP procedures and knowledge of safety and OSHA regulations. Strong interpersonal skills and internal customers and external clients.

**Department:** Research & Development START YOUR APPLICATION (***************************************************************************************************** Do you want to build a stronger, more sustainable future and cultivate your career? Become a part of the Dermalogica Research and Development team. We are looking for a talented **Chemist** to be based at the Corporate Headquarters in Carson working on-site with the R&D department in a temporary capacity. **Role Overview** Seeking a temporary R&D Chemist to support bench scale formulation, batching, and stability placement for skincare products. This is a hands-on, execution focused role supporting active development programs in the lab. **Key Responsibilities** + Prepare bench scale batches following established formulas and SOPs + Support stability setup including labeling, documentation, and sample placement + Accurately record batch data, observations, and deviations + Maintain lab organization, raw material handling, and equipment cleanliness + Partner with formulation and stability teams to support active projects **Required Skills & Experience** + BS in Chemistry, Cosmetic Science, Chemical Engineering, or related field + 1-3 years hands on formulation or lab experience (cosmetics or personal care preferred) + Strong bench skills including weighing, mixing, heating/cooling, and pH adjustment + Familiarity with stability programs and sample tracking + Detail-oriented with strong documentation and organizational skills + Able to work independently with clear direction + Proficient in Microsoft Office (Excel, Word, Outlook) for documentation and data entry **The position is based at the corporate headquarters in Carson, CA,** **and will be fully on-site, 5 days per week (no remote or hybrid).** **The pay rate for this role is $** **35** **per hour** **.** **Ready to make a meaningful impact and advance your career with a global brand revolutionizing the skincare industry?** Apply now and complete your online application. All applications will be reviewed, and our HR team will contact you if your skills align with the position. _Dermalogica is an equal opportunity employer committed to fostering an inclusive culture where all employees are valued, supported, and empowered to succeed._ START YOUR APPLICATION (*****************************************************************************************************

Join a trailblazing startup founded by a renowned Professor in transforming the future of water and air. As a Senior R&D Scientist, you'll be at the heart of pioneering technologies for atmospheric water harvesting and CO2 capture, driving innovations that make a global impact. Why You Should Apply Lead cutting-edge research in atmospheric water harvesting. Competitive salary and benefits package. Collaborate with top-tier scientists and engineers. Play a crucial role in the commercialization of breakthrough technologies. Contribute to sustainability and environmental solutions. What You'll Be Doing: Work with the head of Product Engineering to scale up MOF/COF-based technologies. Collaborate with R&D scientists on technical and functional specifications. Design and develop heat management systems, optimizing components like heat exchangers and thermal storage. Scale technologies from prototype to commercial stage. Optimize system parameters to enhance performance, efficiency, and safety. Evaluate and manage sourcing of materials and components. Set up QC/QA processes and procedures for production. Maintain detailed electronic notebooks and contribute to intellectual property. Report periodically to management and participate in technical meetings. About You: PhD in mechanical engineering or a similar field with a strong research background. Proficient in thermodynamics, fluid mechanics, and heat transfer. Over 5 years of industrial R&D experience. Skilled in designing system-level prototypes and using simulation tools. Familiar with health and safety procedures in production. Excellent teamwork, problem-solving, and communication skills. How To Apply We'd love to see your resume, but we don't need it to have a conversation. Send us an email to *********************** and tell us why you're interested. Or, feel free to email your resume. Please include Job#19433.