Research scientist jobs in Carpinteria, CA - 147 jobs

_corporate_fare_ Google _place_ Goleta, CA, USA **Mid** Experience driving progress, solving problems, and mentoring more junior team members; deeper expertise and applied knowledge within relevant area. **Minimum qualifications:** + PhD in Physics, Material Science or a related field. + 2 years of experience leading a research agenda. + One of more scientific publication submission(s) for conferences, journals, or public repositories (such as CVPR, ICCV, NeurIPS, ICML, ICLR, etc.). + Experience developing and sustaining semiconductor fabrication processes in a cleanroom environment. **Preferred qualifications:** + Experience with multiple, semiconductor equipment (e.g., vacuum, dry etch, PVD/CVD, wet etch, advanced lithography systems, high-volume metrology systems). + Experience with failure analysis techniques (e.g., SEM/EDS, Optical Microscopy, X-Ray, FTIR, XPS). + Experience with micro-fabrication techniques and tools and how these can affect quantum device performance. **About the job** As an organization, Google maintains a portfolio of research projects driven by fundamental research, new product innovation, product contribution and infrastructure goals, while providing individuals and teams the freedom to emphasize specific types of work. As a Research Scientist, you'll setup large-scale tests and deploy promising ideas quickly and broadly, managing deadlines and deliverables while applying the latest theories to develop new and improved products, processes, or technologies. From creating experiments and prototyping implementations to designing new architectures, our research scientists work on real-world problems that span the breadth of computer science, such as machine (and deep) learning, data mining, natural language processing, hardware and software performance analysis, improving compilers for mobile platforms, as well as core search and much more. As a Research Scientist, you'll also actively contribute to the wider research community by sharing and publishing your findings, with ideas inspired by internal projects as well as from collaborations with research programs at partner universities and technical institutes all over the world. The full potential of quantum computing will be unlocked with a large-scale computer capable of complex, error-corrected computations. Google Quantum AI's mission is to build this computer and unlock solutions to classically intractable problems. Our roadmap is focused on advancing the capabilities of quantum computing and enabling meaningful applications. The US base salary range for this full-time position is $166,000-$244,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits. Learn more aboutbenefits at Google (************************************* . **Responsibilities** + Author research papers to share and generate impact of research results across function and in the research community. + Help in growing research business by sharing research trends and best practices within the community. + Drive project work by defining the data structure, framework, design, and evaluation metrics for research solution development and implementation. Identify timelines and obtain resources needed. + Identify new and upcoming research areas by interacting with potential external and internal collaborators. Help in developing long-term research strategy and plans to expand the impact of Google research. + Identify defined problems/gaps in existing technology and engage stakeholders and leaders to address them. Information collected and processed as part of your Google Careers profile, and any job applications you choose to submit is subject to Google'sApplicant and Candidate Privacy Policy (./privacy-policy) . Google is proud to be an equal opportunity and affirmative action employer. We are committed to building a workforce that is representative of the users we serve, creating a culture of belonging, and providing an equal employment opportunity regardless of race, creed, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related condition (including breastfeeding), expecting or parents-to-be, criminal histories consistent with legal requirements, or any other basis protected by law. See also Google's EEO Policy (******************************************************* ,Know your rights: workplace discrimination is illegal (**************************************************************************** ,Belonging at Google (******************************** , and How we hire (**************************************** . If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form (*************************************** . Google is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting. To all recruitment agencies: Google does not accept agency resumes. Please do not forward resumes to our jobs alias, Google employees, or any other organization location. Google is not responsible for any fees related to unsolicited resumes. Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also ******************************* and ************************************************************* If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form: ***************************************

Hewlett Packard Labs -- Senior AI/ML Research ScientistThis role has been designed as ‘Hybrid' with an expectation that you will work on average 2 days per week from an HPE office. Who We Are: Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. We help companies connect, protect, analyze, and act on their data and applications wherever they live, from edge to cloud, so they can turn insights into outcomes at the speed required to thrive in today's complex world. Our culture thrives on finding new and better ways to accelerate what's next. We know varied backgrounds are valued and succeed here. We have the flexibility to manage our work and personal needs. We make bold moves, together, and are a force for good. If you are looking to stretch and grow your career our culture will embrace you. Open up opportunities with HPE. Job Description: While generative AI models, such as Large Language Models (LLMs) and diffusion models, have reached unprecedented results, they are inefficient and lack interpretability, especially when involved in complex reasoning and scientific computing. In the Emergent Machine Intelligence Team at Hewlett Packard Labs, we are dedicated to pushing the boundaries of what's possible with artificial intelligence. As a Senior Research Scientist, you will be at the forefront of our efforts to develop groundbreaking generative AI models. You will be crafting cutting-edge algorithms and applications by augmenting state-of-the-art LLMs with extensive test-time compute, adopting tools from symbolic AI, incorporating physics simulators, and employing insight from statistical physics and non-equilibrium thermodynamics. You will work closely with a multidisciplinary team of engineers, researchers, and product managers, during full development cycles of pre-training, fine-tuning, and inference. Together, our goal is to build scalable, efficient, and innovative generative AI systems. Join us to be a part of a team that shapes the future of high-performance AI. Key Responsibilities: Conduct high-quality research in generative AI, including but not limited to designing algorithms for pre-training and post-training current autoregressive and diffusion models for multimodal data. Design, implement, and validate new algorithms and models for augmented LLMs, pushing the boundaries of AI capabilities. Developing and prototyping novel algorithms for fine-turning, retrieval augmented generation, and in-context learning for various generative models. Developing algorithms for training and inference in Energy-Based Models. Collaborate with cross-functional teams to apply research findings to develop new products or enhance existing ones. Publish research papers in top-tier journals and conferences, sharing findings with the broader scientific community. Stay abreast of the latest AI research and trends, identifying opportunities for innovation and improvement. Mentor junior researchers and engineers, fostering a culture of knowledge sharing and collaboration. Develop prototypes and proof-of-concept implementations to demonstrate the potential of research findings. Engage with the academic community by attending conferences, workshops, and seminars. Required skills and experience: PhD in Computer Science, Artificial Intelligence, Machine Learning, Physics, Mathematics, or other related fields. 5+ years working experience with training and fine-tuning generative AI models including LLMs, diffusion models, or Energy-Based Models Experience with test-time compute techniques, such as chain-of-thoughts, self-consistency, or reinforcement learning based verifiers, etc. Proven track record of research in generative models, demonstrated through first tier publications (e.g., NeurIPS, ICML, ICLR, or high impact journals), patents, or publicly available projects. Proficiency in programming languages commonly used in AI research, such as Python, and experience with AI/ML frameworks (e.g., TensorFlow, PyTorch). Deep understanding of machine learning algorithms and principles, especially in the context of generative AI. Strong mathematical background, with excellent skills in areas such as statistics, probability, linear algebra. Creative and analytical thinking abilities, with a passion for solving complex problems. Excellent communication skills, capable of conveying complex ideas clearly and engaging with both technical and non-technical audiences. Desired skills and experience: Knowledge of computational physics, statistical physics, many-body physics simulations, or quantum computing, and how to apply these principles to develop innovative AI algorithms and models. Proficiency with hosting and operating locally generative AI models, through frameworks such as ollama, vllm, etc. Background in discrete optimization, combinatorial optimization, Monte Carlo methods, quantum-inspired algorithms, and applying these disciplines to enhance AI models. Programming experience in high-performance computing (HPC) environments. Experience with cloud computing platforms, GPU computing, or FPGA computing Additional Skills: Artificial Intelligence Technologies, Cross Domain Knowledge, Data Engineering, Data Science, Design Thinking, Development Fundamentals, Full Stack Development, IT Performance, Machine Learning Operations, Scalability Testing, Security-First Mindset What We Can Offer You: Health & Wellbeing We strive to provide our team members and their loved ones with a comprehensive suite of benefits that supports their physical, financial and emotional wellbeing. Personal & Professional Development We also invest in your career because the better you are, the better we all are. We have specific programs catered to helping you reach any career goals you have - whether you want to become a knowledge expert in your field or apply your skills to another division. Unconditional Inclusion We are unconditionally inclusive in the way we work and celebrate individual uniqueness. We know varied backgrounds are valued and succeed here. We have the flexibility to manage our work and personal needs. We make bold moves, together, and are a force for good. Let's Stay Connected: Follow @HPECareers on Instagram to see the latest on people, culture and tech at HPE. #unitedstates#hpeocto Job: Engineering Job Level: TCP_04 States with Pay Range Requirement The expected salary/wage range for a U.S.-based hire filling this position is provided below. Actual offer may vary from this range based upon geographic location, work experience, education/training, and/or skill level. If this is a sales role, then the listed salary range reflects combined base salary and target-level sales compensation pay. If this is a non-sales role, then the listed salary range reflects base salary only. Variable incentives may also be offered. Information about employee benefits offered can be found at ******************************************************* USD Annual Salary: $133,500.00 - $307,000.00 HPE is an Equal Employment Opportunity/ Veterans/Disabled/LGBT employer. We do not discriminate on the basis of race, gender, or any other protected category, and all decisions we make are made on the basis of qualifications, merit, and business need. Our goal is to be one global team that is representative of our customers, in an inclusive environment where we can continue to innovate and grow together. Please click here: Equal Employment Opportunity. Hewlett Packard Enterprise is EEO Protected Veteran/ Individual with Disabilities. HPE will comply with all applicable laws related to employer use of arrest and conviction records, including laws requiring employers to consider for employment qualified applicants with criminal histories.

The Scientist will support microbiology related methods such as, endotoxin, bioburden, sterility and other compendial methods associated with microbial control. Hands on laboratory work include method troubleshooting, and involvement in evaluating new technologies related to rapid microbiology methods, including developing and executing feasibility and/or validation studies. The candidate will require to work in the laboratory to support feasibility and/or validation studies (time spent in lab varies depending on projects). Experience in pharmaceutical/biotechnology microbiology and manufacturing are preferred. The candidate would be a part of a team that supports various microbiology methods in various stages of the product life cycle. This team supports programs/methods at locations throughout the company. The Scientist collaborates with representatives from key functions within Process Development, Manufacturing, and Quality. Basic Qualifications: Doctorate Degree OR Master's Degree and 4 years of Scientific Experience OR Bachelor's degree and 6 years of Scientific experience Preferred Qualifications: Prior experience in Microbiological Quality at the technical level, including experience with sterile filtration validations Advanced understanding and hands-on experience in various analytical platform such as compendial microbial methods, rapid methods for microbial detection/identification and advanced technologies for detection of bacteria Excellent written and oral communication skills for the timely documentation, presentation and discussion of scientific results in a fast-paced, multi-disciplinary, team-based environment. Advanced ability to critically analyze and interrogate various analytical data sets (e.g. complex dilution schemes) to drive and influence the investigational process Advanced root cause analysis capabilities including leading advanced and complex events Advanced ability to propose and lead new scientific imperatives/initiatives Expert in an investigational laboratory setting within a pharmaceutical or biotechnology company Advanced experience in working closely with scientific and manufacturing disciplines across process development, clinical, and commercial operations Familiarity with cGMP regulations, FDA and EU regulations and guidelines

Employment Type: Contract Business Unit: Biologics Optimization Duration: 1 year with likely extensions 3 Key Consulting is hiring an Associate Scientist for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: The Protein Engineering (PE) group at our client is seeking a highly motivated Associate Scientist to join the Protein Chemistry team at our state-of-the-art research facility in Thousand Oaks, CA. PE is a multidisciplinary team with broad capabilities in protein engineering, expression, purification, and characterization. The ideal candidate should have a strong background in biochemistry and protein purification & analytics, be able to effectively troubleshoot challenging problems, and have strong communication skills. Top Must-Have Skill Sets: Must have Experience with protein purification chromatography techniques (Affinity, IEX, HIC, SEC, etc), liquid chromatography instrumentation (FPLC), software (Unicorn, ChromLab) Must have familiarity with protein analytical techniques (HPLC, MCE, etc…) Analysis software (Chromeleon, LabChip, Empower, etc), preferred Bachelors' degree in Biology, Biochemistry, or related science field Day to Day Responsibilities: Protein purification using a variety of techniques and instrumentation; Protein analytics using a variety of techniques and instrumentation; Contribute to the development of new processes and methods; Capture experimental data in LIMS/ELN systems; Summarize and report results and findings to work group and project teams. Basic Qualifications: Bachelors' degree in Biology, Biochemistry, or a related Life Science field, plus 4 years of experience OR Masters' degree in Biology, Biochemistry, or a related Life Science field, plus 2 years of experience Preferred Qualifications: Experience with protein purification, particularly biologic molecules Expertise with a variety of chromatography techniques, liquid chromatography instrumentation (FPLC) and software (Unicorn, ChromLab) Familiarity with protein analytical techniques (HPLC, MCE, etc…) and analysis software (Chromeleon, LabChip) Knowledge of high throughput purification techniques is a plus Ability to multi-task, work flexibly and efficiently in a cross-functional environment Strong communication and interpersonal skills Red Flags: No protein purification or protein analytics experience Experience in very unrelated fields. No HPLC Interview process: Video Skype Panel Interview: We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

Sansum Diabetes Research Institute has an opportunity for a full-time, board certified, or board-eligible Endocrinologist to serve as a Clinical Research Physician Investigator. SDRI is a non-profit organization and center of excellence with a mission to improve the lives of people impacted by diabetes through research, education, and clinical care. We are a preferred site for industry sponsored clinical trials, a testament to our exceptional research capabilities. On average, SDRI conducts 25+ trials per year, engaging approximately 1,000 participants. Current industry partners include Abbott, Dexcom, Insulet, Eli Lilly, Mannkind, Medtronic Diabetes, Novo Nordisk, Sanofi, Tandem Diabetes Care, and more. We are experts with experience across all study phases, and a broad portfolio of trials and clinical work focused on diabetes and metabolic health. Diversity and inclusivity are prioritized in in our clinical trials---in 2023, 30% of our research participants were from underrepresented populations. We are currently renovating our 18,000 square foot research facility to create a state-of-the-art center where we will accelerate life-changing diabetes research. Position Details: Responsible for 12+ Industry Sponsored Trials Per Year Design, Fund, and Execute Investigator Initiated Trials Develop Strategies and Partnerships to Drive Innovation Across the Enterprise Opportunity to Maintain a Clinical Practice through our Clinics Standard Office Hours Salaried Position: $250,000 - $350,000 Annually NOTE: The listed range is solely a base compensation for experienced full-time physician researchers. It does not include incentives and benefits. The base compensation rate may be adjusted based on training, community need and other possible determining factors. We Offer: Medical/Dental/Vision CME Stipend Malpractice Insurance Disability Retirement 403 (b) Annual Leave and Sick Time Licensure/DEA/Board Exam Fees PSLF Eligibility Requirements: MD or DO with Directly Related Experience in Endocrinology Board Certified or Board Eligible in Endocrinology DEA Certificate Eligible to Work in the United States, Must be in or Relocate to Santa Barbara, CA CA Licensure or the Ability to Obtain CA Licensure Interest in Research, Experience with Research preferred Exceptional Communication and Interpersonal Skills About Santa Barbara: Santa Barbara is known as The American Riviera thanks to its Spanish Colonial Revival architecture, rich heritage, world-renowned food and wine scene, stunning natural beauty and near-perfect weather. We invite you to learn more and to consider joining us at SDRI where you will join an experienced cross-functional team focused on developing and executing trials targeting innovation and excellence crossing drugs, devices, and technology that will impact the health span and life span of people living with diabetes.

Kelly Science & Clinical is seeking **Research Associate, In-Vivo** for a **contract-to-hire** position for a company in **Thousand Oaks, 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 Empowering Experts. **Pay Rate:** $40-45+/hr Depending on experience **Schedule:** Monday-Friday Day Shift **Responsibilities** **:** + Care for research model subjects, primarily rodents + Hands-on in vivo skills performing standard procedures including rodent handling, blood collection, dosing through multiple routes (IV, IP, SC, PO), urine collection, necropsies, and tissue collection in compliance with approved IACUC protocols and AAALAC regulations + Planning breeding, monitoring litters, identifying phenotypes, genotyping, and maintaining specific genetic lines. + Conduct pharmacology studies in multiple animal models to evaluate therapeutic candidates through multiple readouts + Contribute to study design, planning and performing of in vivo studies related to early exploratory indications, tolerability, PK/PD, and therapeutic efficacy + Prepare facilities and sterilize instruments for animal procedures + Work closely with multidisciplinary scientific groups including discovery specialists and in vivo team members + Maintain accurate records of procedures performed on animals + Experience in assessing biomarkers (e.g. Luminex, Western blot, PCR, ELISA ) in animal tissues and cell extracts is preferred **Qualifications:** + BS or MS in a life science discipline with minimum 3 years in vivo experience + Strong in vivo rodent skills including handling and sample collections + Experience with animal colony management is preferred + Familiarity with the basic lab software: Microsoft Office, GraphPad Prism, ELN for record keeping + Excellent organizational skills, knowledge of lab equipment, procedures and day-to-day laboratory function, and strict follow-up of laboratory and vivarium safety guidelines. **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 the Kelly Science & Clinical network. That means our team of expert science & clinical recruiters will have access to your profile, making your opportunities limitless As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Agilent Technologies is a leader in companion diagnostics, partnering with pharmaceutical companies to bring precision medicine therapies to market. The Research Associate will design, plan, and execute stability studies-including accelerated reagent, cut‑section, and stained‑slide stability studies-in support of the development of Companion Diagnostic (CDx) Immunohistochemistry (IHC) assays. Additional responsibilities include: Writing protocols and reports in compliance with Quality Management Systems (QMS), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). Planning study experiment schedules and associated tasks. Performing laboratory experiments while maintaining GLP and GDP standards; making detailed observations; analyzing data; and interpreting results. Presenting results to internal and external cross‑functional project teams. Supporting the Stability team in the development of new templates and processes, as well as in the governance of the Stability team's knowledge repository. As a member of the Stability Team (currently five team members plus one manager), collaborating on cross‑functional project teams that include R&D management, Supply Chain (OFS), and external partners to support development projects and subsequent design transfer into commercial manufacturing. Maintaining a high level of professional expertise through ongoing familiarity with relevant scientific literature. Qualifications Bachelor's or Master's Degree in a biological science or a closely related field. 4+ years of relevant experience, such as planning studies, writing protocols and reports, and performing wet lab experiments. Previous experience in a regulated environment is a plus! IHC, FISH, and/or experience with specific stability studies is highly desired. Previous Medical Device development (R&D) is highly preferred Proficiency in Microsoft Office tools (Word, Excel, PowerPoint, Outlook, OneNote, OneDrive, Teams). Attention to detail and strong organizational skills are a must! Candidates with project management or experience managing multiple laboratory studies with time-sensitive deliverables are highly desired! Strong analytical and critical thinking skills are required. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Ability to prioritize timelines and change priorities. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least February 2, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $88,254.00 - $137,896.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: NoShift: DayDuration: No End DateJob Function: R&D

Senior Research Scientist: Gas Chromatography Mass Spectrometry (GC-MS) Entech Instruments Inc. is a California based instrumentation company is seeking an individual with specialized skills and substantial experience with GC/MS method development. In-depth knowledge of sample preparation and headspace introduction techniques (SPME/SBSE/dynamic Headspace) for a variety of matrices including water, waste water, food and beverage is required. The candidate will participate on a team focused on new product development and new applications for a number of industry verticals including Drinking and Waste Water analysis, Synthetics Characterization, Food, Flavor & Fragrance analysis; Food Safety & Materials; Clinical Breath Analysis, Analysis of Metabolomic Volatile Organic Compounds; Environmental Applications and many more. Entech's newly developed technology VASE (Vacuum Assisted Sorbent Extraction) aims to revolutionize a number of industry's that currently utilize methods such as solvent extraction, dynamic headspace, SPME (Solid Phase Micro-Extraction) and SBSE. The successful candidate will have the opportunity to be involved with R&D product development, applications development, customer application support, app note and peer reviewed paper development and publication, and presenting findings in both oral and poster presentations at conferences and trade shows. Responsibilities: · Researching and investigating major market drivers and duplicating popular analysis utilizing our proprietary sample extraction technology to demonstrate its superiority · Constructing a body of evidence to support the development of an application note and working with other senior chemists to finalize and publish findings · Creating new applications · Web presentations · Method development Requirements : · Minimum of 5 years of GCMS or GCMSMS methods development in a research oriented capacity. · Extensive experience with Thermo GC's a big plus! (ISQ 7000, TSQ 9000, AEI source) · SPME, SBSE, Dynamic Headspace and other sample preparation experience a plus. · Experience with Agilent, Thermo, or Shimadzu GC-MS systems. · Excellent communication skills in English, both oral and written for technical documentation, reporting of experimental results, and oral presentations. · Must be enthusiastic about new product development and willing to participate in rigorous experimentation with short production timelines. · Must be able to present technical concepts and simulated or experimental results. Educational profile should include: Analytical Chemistry at MS or PhD Level. GCMS, GCMSMS, LCMS experience. Entech Instruments offers excellent benefits: 401k Full Medical, Vision, Dental, Life, and Aflac insurance Bonus, Holiday, and PTO Benefits

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice (************************************** and Terms of Use (********************************************* . I further attest that all information I submit in my employment application is true to the best of my knowledge. **Job Description** **About the role** Embedded in our Global Manufacturing Science (GMSci) team, you will provide process science and manufacturing technology leadership for drug product manufacturing across Takeda's global network. You will act as a technical SME for small molecule oral solid dosage and/or parenteral processes, supporting both new product introductions and lifecycle management of marketed products. Working in a matrix environment, you will align cross-functional stakeholders and external partners to enable robust, compliant, and scalable manufacturing. You will also represent the drug product process science perspective in regulatory CMC interactions, translating process understanding into clear and defensible filing content. Overall, you will help strengthen how Takeda applies process knowledge consistently across sites to improve execution and decision-making. **How you will contribute** + Lead and/or oversee DP technical deliverables across the product lifecycle, including: + Technology transfer to internal sites and external contract manufacturing organizations (CMOs) + Process validation planning and execution support + Process characterization and establishment of process understanding + Serve as an escalation point for complex technical investigations and issue resolution, mobilizing and coordinating rapid cross-site support when needed. + Drive manufacturing strategies for assigned key products, ensuring the approach is consistent across Takeda's internal network and CMOs and is grounded in process knowledge and science-based risk management. + Lead continuous improvement for late-phase/matured products by identifying and advancing opportunities that improve robustness, control strategy, and operational performance without compromising compliance. + Partner effectively in a matrix environment with key stakeholders, including: + Pharmaceutical Sciences counterparts (R&D) + Manufacturing site and operating unit leaders + Local Technical Services organizations + Global Quality and Regulatory CMC teams + Ensure process knowledge is captured, shared, and reused across sites and functions to strengthen Takeda's overall DP manufacturing capability and speed decision-making. **What you bring to Takeda** + Degree (BS, MS, and/or PhD) in Chemistry, Chemical Engineering, or a related discipline (or equivalent combination of education and experience). + At least 5 years of relevant industry experience, with experience supporting pharmaceutical development and/or manufacturing in DP-related areas (e.g., OSD and/or parenterals). + Demonstrated success as an SME and project leader in a matrix environment, influencing technical decisions across functions and sites without relying on direct authority. + Strong working knowledge of DP manufacturing technologies, validation and tech transfer principles, and practical application of industry best practices. + Experience contributing to or leading regulatory CMC readiness, including converting process understanding into clear technical narratives and defensible control strategies. + Proven ability to analyze complex problems, drive to root cause, and implement sustainable solutions with high technical rigor. + Communication and stakeholder-management skills that enable effective collaboration, conflict resolution, and alignment across internal teams and external partners. + A working style that prioritizes focus, accountability, and measurable outcomes, while actively building capability for the future. **Takeda Compensation and Benefits Summary** We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. **For Location:** Boston, MA **U.S. Base Salary Range:** $137,000.00 - $215,270.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. **EEO Statement** _Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law._ **Locations** Boston, MABEL - Lessines, Brooklyn Park, MN, CHE - Glattpark (Opfikon) - Zurich HQ, CHE - Neuchatel, IRL - Bray - Production, IRL - Dublin - Baggot Street, IRL - Grange Castle - Production, JPN - Yamaguchi - Hikari Plant, USA - CA - Thousand Oaks - Rancho Conejo **Worker Type** Employee **Worker Sub-Type** Regular **Time Type** Full time **Job Exempt** Yes It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Job: Associate Director/Principal Scientist, CMC Analytical Chemistry Position type: Full Time Reports to: Director of Analytical Chemistry Latigo Biotherapeutics (LatigoBio) is a private, early-stage biotechnology company discovering and developing the next generation of non-opioid medicines for pain and pain-related syndromes to transform the lives of patients. Latigo has a robust pipeline, is well-funded by blue chip investors, and has a highly successful management team and Board of Directors. The company was founded in 2019 and is based in Thousand Oaks, CA. We are science-based, data-driven, patient-focused, and forward-thinking. Position Summary Latigo is searching for an Associate Director/Principal Scientist, CMC Analytical Chemistry. Reporting to the Director of Analytical Chemistry, the candidate will manage preclinical to clinical analytical development activities and oversee the testing and release of drug substance and drug product at contract manufacturers/service providers. The role is responsible for the development, validation and implementation of QC methods for drug substance, drug product, intermediates, starting materials, excipients, and packaging materials at contract manufacturers. Additional responsibilities include reference standard qualification and management, establishment of specifications, oversight of stability programs and the active management and documentation of data. The selected candidate will also work collaboratively with Quality Assurance to assess laboratory conformance with cGMPs, and with CMC Regulatory Affairs to author Module 3 sections of CTD regulatory submissions and written responses to regulatory authorities. Primary Responsibilities Oversee the phase-appropriate analytical activity at contract manufacturers/service providers including analytical method development, qualification and validation for drug substance and drug product. Partner with stakeholders to develop and set specifications for raw materials, intermediates, drug substance, excipients and drug product. Design and manage stability programs for non-GMP and cGMP drug substance and drug product batches and provide guidance for shelf-life and expiry dating. Establish workflows and procedures for analytical and quality control activities. Manage reference standards program, coordinate sourcing, ensure inventory, plan and execute testing and retesting activities, and manage shipments of reference standards. Author, review and approve various analytical reports in a timely manner to support drug substance and drug product development and manufacture, and regulatory filings. Support regulatory submissions by drafting and reviewing analytical sections of INDs, IMPDs, and NDAs, and ensure compliance with current regulatory requirements. Sometimes represent analytical function in CMC teams and project meetings, and work closely with cross-functional teams to meet project timelines and goals. Review/approve controlled cGMP documents, e.g., analytical methods and associated validation protocols/reports, specifications, stability protocols, change controls, LIRs, etc. Manage/perform QC review/approval of analytical test data for IPC testing, drug substance/product batch release and stability test data. Manage and review deviation events and OOS/OOT investigations in coordination with CMC counterparts, QA and regulatory team members. Contribute to the building of CMC infrastructure and company culture. Qualifications and Requirements D. with 8+ years of experience or BS or MS in chemistry or related discipline with 10-15 years of industry experience in an analytical chemistry setting. Good understanding and knowledge of pharmaceutical analytical methods and related issues. Experience with analytical development of small molecules and drug product oral dosage forms from preclinical to late-stage clinical development. Experience managing drug substance and drug product service providers in analytical matters. Extensive knowledge of GLP and cGMP requirements, appropriate regulatory guidance and current industry practices for analytical development. Experience in writing CMC sections for Regulatory submissions (IND experience required; NDA experience highly desirable). Excellent computer skills (e.g., Microsoft Office, Excel, Project). Ability to effectively manage multiple priorities and projects. Preference given to applicants able to work (hybrid) from Thousand Oaks or San Francisco, CA offices.

Company DescriptionJobs for Humanity is partnering with CEDARS-SINAI to build an inclusive and just employment ecosystem. Therefore, we prioritize individuals coming from the following communities: Refugee, Neurodivergent, Single Parent, Blind or Low Vision, Deaf or Hard of Hearing, Black, Hispanic, Asian, Military Veterans, the Elderly, the LGBTQ, and Justice Impacted individuals. This position is open to candidates who reside in and have the legal right to work in the country where the job is located. Company Name: CEDARS-SINAI Job Description Grow your career at Cedars-Sinai! The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes. Join our team and use your experience with an organization known nationally for excellence in research! JOB SUMMARY: Working independently but in close cooperation and in consultation with the Director, Center for Cardiac Arrest Prevention (CCAP), the Research Fellow will be involved in new and ongoing projects at the CCAP. Funded by grants from NIH/NHLBI, the mission of the CCAP is to discover and implement novel clinical tools for prediction and prevention of sudden cardiac arrest, thereby reducing the burden of sudden cardiac death in the community CCAP. Unique opportunities to analyze existing data and publish papers. May develop, adapt, and implement new research techniques and protocols. Analyzes and interprets data. May assist in preparation of grant proposals. Participates in publications and presentations as author or co-author. Not responsible for generating grant funds. ESSENTIAL JOB DUTIES AND RESPONSIBILITIES: - May assist in preparation of grant proposals but is not responsible for generating grant funds. - May participate in publications and presentations as author or co-author. - Designs and performs analyses independently or semi-independently. Will keep appropriate experimental records and documentation and discuss the results with the Principal Investigator. - May develop, adapt, and implement new research techniques and protocols. - Analyzes, interprets, summarizes and compiles data. - Performs routine and complex analyses throughout training period. - May observe MD-patient or MD-human research subject interactions as it pertains directly to research being performed. Educational Requirements: Doctorate (MD) plus clinical cardiology/clinical electrophysiology sub-specialty clinical training for at least two years. Experience: - 1 year experience acquired thorough technical and theoretical knowledge of research project and objectives during one to five (1-5) year post-doctoral appointment - Should have written and published scientific papers. - Has demonstrated aptitude to ask research questions and successfully published papers and/or had grants funded. Physical Demands: - Able to perform moderate lifting. - Able to sit, stand and walk for prolonged periods of time. - Able to read papers and online documents. - Able to operate standard office equipment. - Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions. Working Title: Postdoctoral Scientist - Smidt Heart Institute (Chugh Lab) Department: Heart Institute Operations Business Entity: Cedars-Sinai Medical Center Job Category: Academic/Research Job Specialty: Postdoctoral Position Type: Full-time Shift Length: 8 hour shift Shift Type: Day Base Pay:$64,500.00 - $93,600.00

Our mission is to advance assisted reality by deploying transformative neurotechnology to the people who need it most. At Cognixion, we are building the future of humancomputer interaction through the Cognixion ONE, a regulated medical device that integrates augmented reality with advanced neural and biometric sensing. This wearable system reads and processes brain, eye, and body signals to enable novel control paradigms. Reporting to the VP of Engineering, the Staff Scientistis responsible forthe hands-on development, validation, and translation of product-focused algorithms for CognixionsAR-BCI platform. This role bridges cutting-edgeneuroscience research with robust, production-grade implementations suitable for regulated medical deployment. The ideal candidate thrives equally in the lab and in software, is fluent in modern AI/ML toolchains, and can move seamlessly between biosensing experiments, algorithm development, strategic planning, and communicating research within and beyond the company. Scope of Responsibilities Internal Key Opinion Leader Remain current on advancements in neural sensing, biosignalanalytics, machine learning, and clinical applications. Partner closely with research, engineering, and product teams to identifycompelling algorithmic opportunities, prototype them, validateperformance, and facilitatetranslating successful approaches into production code. Provide detailed input to hardware and software teams regardingproduct requirements, sensing constraints, and clinical application needs. Algorithm & ML Developer Design and execute data-collection protocols to advance Cognixionsneurotechnology platform, including EEG, EMG, EOG, and multimodal biosensing. Analyze data using modern scientific and ML workflows: NumPy/SciPy, Pandas, MNE-Python, MATLAB, scikit-learn, PyTorch, TensorFlow, JAX, and associated visualization libraries (Matplotlib, Plotly, Seaborn). Prototype and implement algorithms in Python, Java, or other mainstream languages as appropriate. Apply classical and advanced signal-processing techniques, including filtering, ICA/PCA, spectral and timefrequency methods, adaptive and spatial filtering, artifact reduction, and model-based approaches. Explore and implement machine-learning and deep-learning models for classification, regression, decoding, multimodal fusion, and real-time inference. Contribute to medical-grade codebases using best practices for reliability, version control, testing, and documentation. Skills & Experience PhD or equivalent experience in engineering, computer science, applied mathematics, neuroscience, or related technical fields. Equivalent industrial experience may be considered; a technical assessment may be required. 10+ years of industry R&D experience, ideally with direct exposure to neurotechnology orbio-signal-based medical products. Demonstrated success shipping at least one product, preferably within regulated medical, neural interface, sensing, or wearable systems. Strong publication and/or patent record showing impactful innovation. Experience translating early-stage research into commercializable, validatedproduct features. Direct experience with biomedical signals (EEG, EMG, EOG, or other non-invasive modalities), data collection, and human-subject experimentation. Deep familiarity with algorithm development, signal processing, ML/AI workflows, and real-time system considerations. Comfortable leading experiments, designing studies, validatingresults statistically, and communicating findings to multidisciplinary teams.

Are you a passionate scientist ready to push the boundaries of research and development? Join our dynamic R&D team as an R&D Scientist I, where you ll spearhead groundbreaking experiments, analyze cutting-edge data, and contribute to revolutionary product advancements. If you thrive in a collaborative environment and are driven by discovery, we want you on our team! Who is Meissner? The goal at Meissner is to be more than simply good; it is to be extraordinary. Extraordinary performance comes from extraordinary people. Meissner as a group is passionate about helping our clients manufacture lifesaving and life enhancing drugs, therapies, and vaccines. We develop, manufacture, supply and service advanced microfiltration products and single-use systems worldwide. We know that when you are passionate about what you do, it s more than just a job. Meissner is focused on the development of the whole individual, and we have programs and tools in place to help us stay at our best mentally and physically. In alignment with our commitment to support the growth and development of the whole individual, Meissner has inaugurated a Learning and Development department to solely focus on cultivating our team. When you grow, we grow. How you will make an impact: At Meissner, we provide B2B technical solutions, that are deployed to improve the human condition. Our customers use our products and technologies to develop new therapeutics and many familiar products that support our modern lifestyle. At the core of these products, are in-house technologies that are developed and maintained by highly talented and self-driven engineers and scientists. Contributing to formulations, material testing, and recommendations while correlating material properties and filtration studies to processes. Developing new filters, filtration membranes and application-specific products to meet emerging technological needs. Managing projects with a focus on deliverables, knowledge sharing, and collaboration across teams to ensure successful outcomes. We are looking for a self-driven candidate who is motivated to make an impact in the development of new technologies and join a dynamic entrepreneurial team.. The R&D Scientist I independently plans and executes scientific experiments to develop innovative products, improve processes, and generate data that supports technical and business objectives. This role contributes scientific insight, leads segments of R&D projects, and supports cross-functional collaboration to drive innovation and commercialization. Design, execute, and analyze complex experiments with minimal supervision. Develop and optimize formulations, processes, and analytical methods. Interpret data and translate results into actionable recommendations. Hands-on experimental work involving the characterization of material properties. Process development work in the laboratory involving testing equipment, chemical processes, and testing materials and products (membranes, filters, polymers, etc.). Carry out filter testing, failure analysis, lifetime studies, comparative performance evaluations using appropriate instrumentation that may involve chemical analysis, microscopy, thermal and mechanical properties evaluation. This is an on-site role based out of our headquarters in Camarillo, CA. The skills and experience you ll need: Master s degree required in STEM-related field that is relevant to the operations of the company with 2+ years of relevant experience or PhD with 1+ years of experience. Strong foundation in relevant scientific principles and laboratory techniques. Proficiency with different laboratory instrumentation used in characterizing material properties. Experience in experimental design, statistical analysis, and technical problem-solving. Proven capabilities in writing effective reports and data analysis. Excellent attention to detail and documentation practices. Don t meet every single requirement? Apply anyway. What we can offer you: Full Medical, Dental and Vision coverage with HSA Employer Contributions for eligible plans Additional Perks- HQ Onsite Full Gym, Ultramodern Coffee Bars, Free EV Charging Stations, Employee Discounts 401k, Profit Sharing, 401k Advisory Services Company Sponsored Life Insurance Employee Assistance Program Paid Time Off, Paid Holidays, Anniversary Holiday Ready to make an impact? Let s talk. This position may require you to access information that is subject to U.S. export regulations. You may only access such information if you are a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. government. Meissner is proud to be an Equal Opportunity Employer. US BASE PAY SCALE $87,500 - $108,000 The base pay scale for this role is what Meissner reasonably expects to pay for the position although actual pay may vary from this scale depending on an applicant's experience.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description Job Summary: Responsible for providing support to the Process Analytics group, a unit within the Digital Integration & Predictive Technologies (DIPT) organization in Process Development. The position will be based in Thousand Oaks, CA. Support will include organizing and interpreting lab data, analyzing results using statistical techniques. The responsibilities also include performing laboratory experiments including unit operations set up, calibration of various lab tools, sampling and data acquisition from primary or secondary data sources with minimal supervision. Basic Qualifications • Bachelor's degree OR • Associate's degree & 4 years of directly related experience OR • High school diploma / GED & 6 years of directly related experience Preferred Qualifications • B.Sc., in Chemical, Biochemical Engineering or Life Sciences, preferably with expertise in bio/pharmaceutical processes. • Practical experience and interest in multivariate data analysis and predictive modeling. • Experience working with large data sets, data mining and machine learning tools. • Experience in Matlab or R Programming Languages and basic Microsoft tools. • Understanding of biopharmaceuticals process, related unit operations including analytical methods and process controls. • Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy • Independent, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration. • Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making • Solid leadership, technical writing, and communication/presentation skills. Qualifications Basic Qualifications • Bachelor's degree OR • Associate's degree & 4 years of directly related experience OR • High school diploma / GED & 6 years of directly related experience Preferred Qualifications • B.Sc., in Chemical, Biochemical Engineering or Life Sciences, preferably with expertise in bio/pharmaceutical processes. • Practical experience and interest in multivariate data analysis and predictive modeling. • Experience working with large data sets, data mining and machine learning tools. • Experience in Matlab or R Programming Languages and basic Microsoft tools. • Understanding of biopharmaceuticals process, related unit operations including analytical methods and process controls. • Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy • Independent, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration. • Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making • Solid leadership, technical writing, and communication/presentation skills. Additional Information All your information will be kept confidential according to EEO guidelines.

Microsoft Quantum has assembled a talented and diverse international team to create the world's first scalable quantum computing system. Our full-stack approach involves exciting innovation from the physics at the quantum plane to providing global quantum services. The Microsoft Quantum program strives to fundamentally change the world of computing to help solve humankind's currently unsolvable problems. We are on the cusp of an accelerated effort in quantum computing. We are looking for a Principal Researcher. This position offers an opportunity to have a meaningful influence on a revolutionary technology. The research and development effort includes a diverse staff of theoretical and experimental physicists, hardware designers and software engineers around the world. For more information about the Microsoft Quantum team, please visit ****************************** Microsoft's mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond. Responsibilities * Design and develop novel fault-tolerance strategies for quantum computing systems, working in close collaboration with a multidisciplinary team of theorists and experimentalists. * Advance the theory and implementation of quantum error correction codes, contributing to the development of both logical and physical qubit architectures. * Drive research and experimentation aimed at building scalable, resilient quantum computers capable of delivering practical value. * Engage in creative problem-solving and cross-functional collaboration to overcome technical challenges in quantum system design. * Foster a culture of collaboration, creativity, and technical excellence while embodying. * Other: * Embody our Culture and Values Qualifications Required qualifications: * Doctorate in relevant field AND 3+ years related research experience * OR Master's Degree in relevant field AND 4+ years related research experience * OR Bachelor's Degree in relevant field AND 6+ years related research experience * OR equivalent experience. Other Requirements: * Ability to meet Microsoft, customer and/or government security screening requirements are required for this role. These requirements include, but are not limited to the following specialized security screenings: * Microsoft Cloud Background Check: This position will be required to pass the Microsoft Cloud Background Check upon hire/transfer and every two years thereafter. * Citizenship & Citizenship Verification: This role will require access to information that is controlled for export under export control regulations, potentially under the U.S. International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR), the EU Dual Use Regulation, and/or other export control regulations. As a condition of employment, the successful candidate will be required to provide either proof of their country of citizenship or proof of their U.S. permanent residency or other protected status (e.g., under 8 U.S.C. § 1324b(a)(3)) for assessment of eligibility to access the export-controlled information. To meet this legal requirement, and as a condition of employment, the successful candidate's citizenship will be verified with a valid passport. Lawful permanent residents, refugees, and asylees may verify status using other documents, where applicable. Additional or Preferred Qualifications: * Doctorate in relevant field AND 5+ years related research experience * OR Master's Degree in relevant field AND 8+ years related research experience * OR Bachelor's Degree in relevant field AND 12+ years related research experience * OR equivalent experience. * Demonstrated ability to communicate clearly and collaborate effectively with individuals from diverse backgrounds and teams. * Ability to approach problems thoughtfully and with attention to detail, considering multiple perspectives and potential solutions. * Ability to apply AI to accelerate engineering while developing shipping & prototype code. * Ability to leverage AI tools to drive innovation and efficiency (e.g., performance modeling and analysis, research gathering, day to day task automation). * Experience publishing academic papers as a lead author or essential contributor. * Experience participating in a top conference in relevant research domain. * Experience with quantum error-correction, fault-tolerant quantum computing, and/or QCVV. #QuantumCareers #MDQCareers Research Sciences IC5 - The typical base pay range for this role across the U.S. is USD $139,900 - $274,800 per year. There is a different range applicable to specific work locations, within the San Francisco Bay area and New York City metropolitan area, and the base pay range for this role in those locations is USD $188,000 - $304,200 per year. Certain roles may be eligible for benefits and other compensation. Find additional benefits and pay information here: **************************************************** This position will be open for a minimum of 5 days, with applications accepted on an ongoing basis until the position is filled. Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance with religious accommodations and/or a reasonable accommodation due to a disability during the application process, read more about requesting accommodations.

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Performs laboratory experiments related to development of robust upstream processes for manufacturing of human therapeutic proteins produced in recombinant mammalian cells and bacteria. Designs, executes, and analyzes experiments at laboratory scale, including shake flasks, spin tubes, scale down bioreactor systems (Ambr) and bench top reactors (Applikon). Develops and characterizes scaled-down models for upstream unit operations. Responsible for accurate laboratory data entry, lab maintenance and upkeep, and report writing. Supports identification and optimization of alternative laboratory methods and/or equipment to improve work efficiency and throughput. Retains an up to date knowledge of analytical techniques and relevant scientific literature. Keeps Team Leader & Project Manager informed on a regular basis on project status and any circumstances which may alter project scope or established timelines. Qualifications BS in Cell Biology, Molecular Biology, Biochemistry, Chemical Engineering or other relevant area. 1-5 years relevant laboratory experience. Knowledge of and experience with cell culture techniques; cell handling, aseptic technique, cell counting, media preparation, pipetting, centrifugation, filtration, etc. Knowledge of technologies related to protein expression. Experience in cell culture process development and Design of Experiment (DOE) a plus. Knowledge of bacterial fermentation is a plus. Theoretical knowledge and some practical experience in cell culture as demonstrated by presentations and/or publication record. Participates in solving difficult and complex technical problems. Good communication and presentation skills. Team player. Develop solutions to a variety of complex problems. Solutions are imaginative, practical and consistent with organization objectives. Plan schedules and lab activities to accomplish objectives. Ability to track and execute on multiple projects simultaneously. Creative, actively participate in idea generation. Additional Information If you are not interested in looking at new opportunities at this time I fully understand. I would in that case be appreciative of any referrals you could provide from your network of friends and colleagues in the industry. we do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job. Kind Regards Dipti Ghodke Senior Technical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732 - 844 -8719 (W) # 732-549-2030 - Ext - 315 www.irionline.com LinkedIn: https://in.linkedin.com/in/diptighodke Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

**Duration:** **06** **months of contract** **Shift** : 8-5 PM Hybrid set up: All candidates must be willing to work 5 days onsite when needed but can also be a remote depending on the schedule or agreement with the hiring manager. **Job Description:** The candidate will require to work in the laboratory to support feasibility and/or validation studies (time spent in lab varies depending on projects). Experience in pharmaceutical/biotechnology microbiology and manufacturing are preferred. The candidate would be a part of a team that supports various microbiology methods in various stages of the product life cycle. This team supports programs/methods at locations throughout the company. The Scientist collaborates with representatives from key functions within Process Development, Manufacturing, and Quality. **Responsibilities:** + This position is being opened to support sterile filtration validation testing. This is a new job responsibility for my team. Team member will assist with developing methods, creating documents to support this work. This team member will also be assisting in the execution/testing of sterile filter validations + The candidate will require to work in the laboratory to support feasibility and/or validation studies (time spent in lab varies depending on projects). Experience in pharmaceutical/biotechnology microbiology and manufacturing are preferred. + The candidate would be a part of a team that supports various microbiology methods in various stages of the product life cycle. This team supports programs/methods at locations throughout the company. The Scientist collaborates with representatives from key functions within Process Development, Manufacturing, and Quality. **Top must have Skills:** + Experience with Microbiology methods such as Endotoxin, Bioburden and Sterility + Experience with Sterile Filter Validation (working with Brevundimonas diminuta) + Experience working at a biopharmaceutical manufacturing site **Basic Qualifications:** + Doctorate degree OR + Masters degree and 2 years of experience OR + Bachelors degree and 4 years of experience **Preferred Qualifications:** + Prior experience in Microbiological Quality at the technical level, including experience with sterile filtration validations + Advanced understanding and hands-on experience in various analytical platform such as compendial microbial methods, rapid methods for microbial detection/identification and advanced technologies for detection of bacteria + Excellent written and oral communication skills for the timely documentation, presentation and discussion of scientific results in a fast-paced, multi-disciplinary, team-based environment. + Advanced ability to critically analyze and interrogate various analytical data sets (e.g. complex dilution schemes) to drive and influence the investigational process + Advanced root cause analysis capabilities including leading advanced and complex events + Advanced ability to propose and lead new scientific imperatives/initiatives + Expert in an investigational laboratory setting within a pharmaceutical or biotechnology company + Advanced experience in working closely with scientific and manufacturing disciplines across process development, clinical, and commercial operations + Familiarity with cGMP regulations, FDA and EU regulations and guidelines **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, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"

We are seeking a dedicated Senior Scientist to join our oncology research team in Thousand Oaks, CA. This is a fully onsite position with working hours from 8:30 AM to 5 PM, Monday through Friday. The role involves contributing significantly to the discovery and development of small-molecule therapeutics within the Department of Oncology Research. Responsibilities + Plan, conduct, and monitor experiments with minimal supervision. + Record, organize, and analyze experimental data to generate robust and reliable results. + Transfer experimental methods from literature to the lab and implement necessary modifications. + Develop and implement new protocols with moderate review. + Engage in scientific discussions with coworkers and communicate data and interpretations to the work group. + Ensure quality data through developed systems and troubleshoot equipment and experimental difficulties. + Contribute to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions, and/or patents. + Participate in department-wide support efforts such as safety, recruiting, and committees. + Train staff and/or supervise others as needed. + Coordinate and organize resources required to complete tasks. + Understand when to seek input and when to make independent judgments. Essential Skills + PhD in Cancer Biology, Genetics, or a related field with hands-on experience in mammalian cell culture and standard molecular biology techniques, or MS with 3-5 years of relevant industry experience. + Strong data analysis skills and scientific independence. + Demonstrated publication record, preferably including first-author work for PhD candidates. + Proficiency in standard cell and molecular biology experimental design and techniques such as mammalian cell culture, western blotting, molecular cloning, qPCR, and flow cytometry. Additional Skills & Qualifications + Research experience in cancer biology, genetics, or a related field. + Excellent organizational, interpersonal, and communication skills. + Experience with data analysis tools such as GraphPad Prism. Work Environment The work takes place in an onsite oncology research lab with a focus on mammalian tissue culture and molecular biology. The position operates within standard laboratory conditions and requires proficiency in various laboratory instruments and techniques. Collaboration and communication are key, as is the ability to work independently and effectively troubleshoot issues as they arise. Job Type & Location This is a Contract position based out of Thousand Oaks, CA. Pay and Benefits The pay range for this position is $44.00 - $47.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Thousand Oaks,CA. Application Deadline This position is anticipated to close on Feb 4, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Employment Type: Contingent Worker (Contract, W2) Contract Length: 6 months (possible extension) Compensation: $30/$35 per hour (based on experience) Summary of the Role Join a big biopharma leader's Translational Safety & Bioanalytical Sciences organization as a Nonclinical Report Quality Control Associate. In this vital onsite role, you will provide quality control of nonclinical reports generated by scientific staff, ensuring data integrity and regulatory compliance. You will interact with cross-functional teams to review documents and verify data accuracy, supporting critical filings. Key Responsibilities Verify accuracy of experimental data in written reports against summary analysis files and electronic lab notebooks (ELNs) Ensure data within reports accurately reflect ELN sources and provide traceability to internal data repositories Coordinate and support the quality control (QC) process by accessing multiple internal databases (ELN, CDOCs, RIM, LIMS, etc.) Confirm presence of supporting data files in approved storage locations Ensure compliance with company report formatting and proofreading standards Own the QC review for toxicology and pharmacokinetic (non-GLP) study reports to support regulatory filings Assist with report formatting to meet regulatory filing requirements Required Experience & Skills Experience in quality control or review of nonclinical scientific reports Familiarity with laboratory data sources and regulatory documentation Demonstrated attention to detail and data integrity Strong organizational skills and ability to handle multiple priorities Proficiency with MS Office tools including Word, Excel, PowerPoint, Visio, and Outlook Preferred Qualifications Ability to solve complex technical problems independently in a fast-paced environment Effective verbal and written communication and interpersonal skills Working knowledge of regulatory (GLP and GCP) and pharmaceutical processes Top 3 Must Have Skills 1. Ability to solve complex technical problems and work independently in a fast-paced environment 2. Effective verbal and written communication and interpersonal skills 3. Attention to detail Day-to-Day Responsibilities Review reports for accuracy versus lab data and source files Verify formatting and regulatory compliance of submitted documents Coordinate with scientific staff to resolve discrepancies Maintain thorough QC records and documentation Basic Qualifications Master's degree and/or 1+ years of related laboratory support experience Bachelor's degree and/or 2+ years of related laboratory support experience Associate degree and/or 4+ years of related laboratory support experience High school diploma or GED and 6 years of related laboratory support experience Complete understanding of technical principles and concepts to perform a wide range of work in a role This posting is for Contingent Worker, not an FTE