Research Scientist Jobs in Carpinteria, CA

Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do. Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Principal Scientist - Safety PharmacologyWhat you will do Lets do this. Lets change the world. The Translational Safety and Bioanalytical Sciences (TS&BA) function at Amgen is seeking candidates for the position of Principal Scientist to join our Safety Pharmacology Sciences (SP Sci) team based in Thousand Oak, CA. The SP Sci team supports the Amgen portfolio from target identification through clinical development, with an emphasis on developing translational safety strategies to support project teams and various drug modalities. The Principal Scientist will be part of an expert team dedicated to the development of small molecules, oligonucleotides and protein therapeutics in close collaboration with toxicologists, pathologists, and scientists within the organization. In this vital role, you will design and perform in vitro assays for various projects and present the work to cross-functional teams. Additionally, multiple opportunities exist for the new hire to grow their career by leveraging their subject matter expertise to innovate (i.e., new model development), collaborate with other members of the SP Sci team (i.e., present key finding at internal/external meetings), and engage with drug discovery project teams (i.e., advance new molecules into clinical development). Responsibilities: Serve as an in vitro and ex vivo electrophysiologist, supporting investigative activities by employing electrophysiology techniques (conducted internally or outsourced) to assess the impact of test compounds on ion channels, cells, and isolated tissues, such as the isolated perfused heart. Provide subject matter expertise in developing fit-for-purpose translational safety strategies to address new challenges within the Amgen drug pipeline. The successful candidate will have an in-depth understanding of ion channel biophysics and pharmacology (especially cardiac) with proven ability to apply this knowledge in the development and validation of assays related to ion channel and cardiac function. The candidate will hold subject matter expertise in a particular area which could include use of hi PSC-derived cardiomyocytes for compound screening, dissociated primary cells, or heterologous mammalian cell expression systems, and techniques such as patch clamp, multielectrode array (MEA) recording or calcium imaging. Experience with artificial intelligence, machine learning, and/or programming would be advantageous. The candidate should have a results-focused attitude, with a track record of independent critical thinking and scientific achievement in the area of electrophysiology The candidate should have strong verbal and written communication skills, be highly motivated, creative and collaborative, with the ability to work in a team environment. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a subject matter expert with these qualifications. Basic Qualifications: Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] in a relevant scientific discipline (e.g. physiology or pharmacology) and 2 years of electrophysiology experience. Or Masters degree and 5 years of electrophysiology experience. Or Bachelors degree and 7 years of electrophysiology experience. Preferred Qualifications: Pharmaceutical industry electrophysiology experience. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models, including remote and hybrid work arrangements, where possible Apply now and make a lasting impact with the Amgen team.careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. #J-18808-Ljbffr

Apply remote type On Site locations US - California - Thousand Oaks time type Full time posted on Posted 2 Days Ago job requisition id R-203821 Career Category Research Job DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller, happier lives. Our award-winning culture is collaborative, innovative, and science-based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do We are building upon our solid Cardiovascular foundation and long-term dedication to patients by developing a whole new class of novel molecules. We are seeking a dedicated and highly motivated Principal Scientist to become a member of the Department of Cardiometabolic Disorders within Amgen Research located in Thousand Oaks, CA. In this vital and exciting role you will be an ideator and drug hunter and are expected to conduct biology research and identify therapeutic targets in cardiometabolic disease that are tractable and offer the opportunity of delivering disease-modifying potential in patients. The proposal and advancement of a drug discovery program will be based on a sound and compelling scientific rationale that may include validation from human genetics and/or clinical studies. Critical thinking, ingenuity, the ability to design and conduct mechanistic studies and deep biology, technical proficiency, excellent communication skills, integrity and the ability to work in a multi-disciplinary environment will be critical toward advancing programs in the cardiometabolic pipeline. You will initially work at the bench conducting in vivo and/or in vitro preclinical studies with a focus on PAH, vascular disease and/or heart failure. Over time, you will also demonstrate strong leadership skills and the ability to manage a team of scientists conducting drug discovery research. As part of the team, the candidate may also support other new and existing drug discovery programs in the department to help advance the best assets in the Cardiometabolic Disorders portfolio. Conceptualizing and proposing therapeutic targets for the treatment of cardiometabolic disease Designing and performing in vitro and cell-based experiments Independently performing data analysis and interpreting results Communicating scientific results through written and oral presentations Collaborating with teams from other functions in the company to advance our programs Documenting work through written protocols, electronic laboratory notebooks and study reports. Advising colleagues in areas of expertise What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a scientist with these qualifications. Basic Qualifications: Doctorate degree and 2 years of scientific experience Or Master's degree and 5 years of scientific experience Or Bachelor's degree and 7 years of scientific experience Preferred Qualifications: PhD with postdoctoral experience in cardiometabolic disease (industry experience is strongly preferred) Strong target ideation capabilities and critical thinking to enable discovery of innovative medicines for patients Exceptional in vivo and/or in vitro pharmacology skills and capability to independently design, implement and analyze studies with proper controls and generate reproducible high-quality data Technical mastery of general molecular biology, biochemical, and cell-signaling techniques including immunoblotting, immunocytochemistry, RT-qPCR, immunoprecipitation, and ELISA Basic knowledge of statistical methods applied in a consistent and rigorous manner to all data sets generated Excellent written and oral communication skills and interpersonal skills that enable effective team interactions and communication of key data to all key stakeholders A strong ability to collaborate cross-functionally in a multidisciplinary environment is critical Capability to deliver high quality manuscripts, posters and presentations for internal and external peer-reviewed publication and conference attendance. Understanding of human genetics and genomic data mining for target identification are a plus. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models, including remote and hybrid work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Salary Range 135,729.00 USD - 168,454.00 USD About Us Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. #J-18808-Ljbffr

Senior Scientist/Principal Scientist - CNS Drug Delivery Our client is a cutting-edge neuroscience company developing innovative brain shuttle technology aimed at revolutionizing the delivery of drugs and molecules to the brain. This proprietary platform is designed to overcome the blood-brain barrier and provide groundbreaking solutions for treating Alzheimer's disease, neurodegenerative disorders, and psychiatric conditions. As a well-funded biotech firm, they offer a unique opportunity to join a highly dynamic team dedicated to advancing CNS drug delivery technologies. We are seeking a Senior Scientist/Principal Scientist to lead bioanalytical and biodistribution studies, manage IND-enabling efforts, and contribute to the development of this novel brain shuttle platform. Job Specifications: Job Type: Full-time Company: Leading Neuroscience Biotech Company Location: Thousand Oaks Pay Rate: $160,000 annually (flexible for highly experienced candidates) Shift: Day Shift Roles and Responsibilities: Lead and execute bioanalytical and biodistribution studies to advance CNS drug delivery platforms. Develop and validate assays for quantifying drug levels in plasma, brain, and other tissues. Design and interpret Pharmacokinetic/Pharmacodynamic (PK/PD) studies to evaluate drug delivery, efficacy, and safety. Manage IND-enabling studies, collaborating closely with internal teams and external CRO partners to ensure timely execution and compliance. Mentor and guide junior scientists, fostering a collaborative and innovative research environment. Stay abreast of the latest scientific advances in CNS drug delivery, bioanalysis, and regulatory frameworks to ensure research practices are aligned with industry standards. Qualifications & Skills: Education: PhD in a life sciences field (e.g., Neuroscience, Pharmacology, Biology) or related discipline. Experience: 8-10+ years of industry experience in bioanalytics, biodistribution, and PK/PD studies, ideally with large molecules (antibodies, oligonucleotides, peptides). CNS-related experience is highly preferred. Proven track record of managing IND-enabling studies and working effectively with CROs. Expertise in blood-brain barrier biology and CNS drug delivery technologies. Strong background in bioanalytical methods, including ELISA, RT-qPCR, and histology. Excellent problem-solving skills, scientific rigor, and the ability to thrive in a fast-paced, dynamic research environment. Experience in managing and mentoring scientific teams, with a focus on study design and execution rather than performance reviews. Opportunities: Lead pioneering research in CNS drug delivery, contributing to the development of transformative therapeutics for neurodegenerative and psychiatric disorders. Collaborate with a talented and driven team of scientists to push the boundaries of biotechnology and neuroscience. Potential for career advancement within a rapidly growing, well-funded biotech company at the forefront of drug delivery innovation. Company Culture: Join a dynamic, passionate team at a cutting-edge neuroscience company where creativity, collaboration, and scientific excellence drive our mission. Our supportive work environment empowers team members to explore new ideas, grow professionally, and contribute to making a lasting impact on healthcare solutions for neurodegenerative diseases.

Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Principal Scientist - Safety PharmacologyWhat you will do The Translational Safety and Bioanalytical Sciences (TS&BA) function at Amgen is seeking candidates for the position of Principal Scientist to join our Safety Pharmacology Sciences (SP Sci) team based in Thousand Oak, CA. The SP Sci team supports the Amgen portfolio from target identification through clinical development, with an emphasis on developing translational safety strategies to support project teams and various drug modalities. The Principal Scientist will be part of an expert team dedicated to the development of small molecules, oligonucleotides and protein therapeutics in close collaboration with toxicologists, pathologists, and scientists within the organization. In this vital role, you will design and perform in vitro assays for various projects and present the work to cross-functional teams. Additionally, multiple opportunities exist for the new hire to grow their career by leveraging their subject matter expertise to innovate, collaborate with other members of the SP Sci team, and engage with drug discovery project teams. Responsibilities: Serve as an in vitro and ex vivo electrophysiologist, supporting investigative activities by employing electrophysiology techniques to assess the impact of test compounds on ion channels, cells, and isolated tissues, such as the isolated perfused heart. Provide subject matter expertise in developing fit-for-purpose translational safety strategies to address new challenges within the Amgen drug pipeline. The successful candidate will have an in-depth understanding of ion channel biophysics and pharmacology with proven ability to apply this knowledge in the development and validation of assays related to ion channel and cardiac function. The candidate will hold subject matter expertise in a particular area which could include use of hi PSC-derived cardiomyocytes for compound screening, dissociated primary cells, or heterologous mammalian cell expression systems, and techniques such as patch clamp, multielectrode array (MEA) recording or calcium imaging. Experience with artificial intelligence, machine learning, and/or programming would be advantageous. The candidate should have a results-focused attitude, with a track record of independent critical thinking and scientific achievement in the area of electrophysiology. The candidate should have strong verbal and written communication skills, be highly motivated, creative and collaborative, with the ability to work in a team environment. What we expect of you The dynamic professional we seek is a subject matter expert with these qualifications. Basic Qualifications: Doctorate degree PhD OR PharmD OR MD in a relevant scientific discipline (e.g. physiology or pharmacology) and 2 years of electrophysiology experience. Or Master's degree and 5 years of electrophysiology experience. Or Bachelor's degree and 7 years of electrophysiology experience. Preferred Qualifications: Pharmaceutical industry electrophysiology experience. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan. Stock-based long-term incentives. Award-winning time-off plans. Flexible work models, including remote and hybrid work arrangements, where possible. Apply now and make a lasting impact with the Amgen team.careers.amgen.com Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. #J-18808-Ljbffr

Apply share * link Copy link * email Email a friend Minimum qualifications: * PhD in physics, electrical engineering or equivalent experience. * Experience designing, constructing, or maintaining scientific apparatuses (e.g., cryostats, microscopes, electronics, sample packages, microwave signal chains, optical setups). * Experience working in multiple disciplines (fabrication, electronics, software, cryogenics, modeling, measurement) in support of project goals. * Experience using software for scientific apparatus control and data analysis. Preferred qualifications: * Experience with microwave, RF, optoelectronic, optomechanical or optical control or measurement. * Experience with control or characterization of quantum devices. * Experience with cryogenic or vacuum environments and equipment. * Experience with design and layout of microfabricated devices. * Experience publishing in scientific journals or presenting at conferences. 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 $141,000-$202,000 + 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 about benefits at Google. Responsibilities * Characterize the performance of readout and reset in superconducting qubit devices and work with theorists to model their behavior. * Write software implementing characterization and other experiments, and work with automation experts to merge that software into a mainline automated calibration and characterization system. * Conceive of and develop readout and reset hardware. * Communicate scientific results to the Quantum AI team and to the broader scientific community. * Through conferences and literature review, investigate and report on technological advances from academia and elsewhere that may enable faster, more accurate, and larger scale readout and reset.

Employment Type: Contract Duration: 12 months with likely extensions Note: Remote and onsite 3 Key Consulting is hiring a Specialist IS Analyst for a consulting engagement with our direct client, a leading global bio-pharmaceutical company. Job Summary: Associate Scientist Attribute Sciences Process Development Group performs analytical testing of process related impurities to support development of large molecules in pipeline. We provide essential data to purification scientists regarding clearance of process related impurities and develop methods and transfer them to various analytical laboratories including Quality Control for release testing of clinical and commercial materials. Ideal candidate: M.S. or B.S. with 2 years of work/industry experience in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field. Experience with ELISA assays required. Responsibilities: Generating, analyzing, and interpreting analytical data Supporting analytical projects involving method development, qualification, and transfer Top Must have Skill Sets: ELISA experience required Prior hands-on lab experience Good communication Pipetting skills Day-To-Day Responsibilities: Analyzing routine samples by ELISA, data interpretation and reporting, documentation of results and peer review of electronic notebooks. Employee Value Proposition: The person in this role will run routine samples and some method trouble shooting, report results and reviewing other scientists' work. Red Flags: No ELISA experience Frequent movement between companies/jobs Interview Process: Initial phone screen with hiring manager then video interview with other team members We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this position, please feel free to look at other positions on our website *********************** You are welcome to also share this posting with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Scientist - Cardiometabolic Disorders What you will do Let's do this. Let's change the world. Amgen is seeking an enthusiastic, collaborative Associate Scientist to join our drug discovery team in the Cardiometabolic Disorders Research Therapeutic Area in Thousand Oaks, CA In this vital role you will be working in the laboratory on experiments and presenting results to the team. Well-suited applicants will have broad laboratory training, deep scientific curiosity and a positive approach working in a team-based research environment. The successful candidates should have significant experience in molecular and cellular biology techniques and performing in vitro assays. Conduct laboratory experiments Analyze data, communicate results & develop solutions to technical problems Additional Qualifications/Responsibilities What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is an enthusiastic scientist with these qualifications. Basic Qualifications: Bachelor's degree in related field with academic or industrial lab experience OR Associate's degree and 2+ years of laboratory-based research experience in academic or industrial labs Preferred Qualifications: Master's degree and 1+ years of relevant experience Educational or practical experience related to obesity research Hands on experience with molecular and cellular biology techniques including RNA and protein extraction and analysis, quantitative PCR and mammalian cell culture Hands on experience and knowledge in developing, validating and executing cell-based and biochemical assays, including ELISA/immunological assays and cAMP assays Organizational and notebook/record keeping skills Highly motivated, creative, collaborative and detail-oriented Effective verbal and written communication skills Work effectively in a highly collaborative research environment Computer literacy, e.g., GraphPad Prism, Excel, PowerPoint and Word What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models, including remote and hybrid work arrangements, where possible Salary Range 99,105.00 USD - 115,592.00 USD

**Be visionary** Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. **Job Description** **Job Summary:** Teledyne FLIR is seeking a Sr. Research Scientist for Detector Product Development: + Assist in making strategic decisions on design and development of product line + Lead and support semiconductor process development efforts. + Assist as a technical lead on resolving developmental and production related issues **Primary Duties & Responsibilities:** + Project Management: Responsible for assisting in the oversight and management of technical aspects of strategic programs. + Projects are typically internally funded or supported by a customer-issued development contract, most of which are with US Government agencies or large prime contractors. + May provide oversight of some aspects of projects, including progress towards technical milestones, monitoring costs and labor expenditures relative to the project's budget, support contractual reporting requirements, business development by working to secure add-on funding or expanded scope. + Advance Detector Developments + Support efforts in developing high performance, low dark current detector arrays along with their integration into focal plane arrays. + Assist in device improvements through device design, growth, and processing. + Assist in the development hybridization processes for integrating small pixel, large arrays with silicon readout integrated circuits (ROIC). + Overall, build off existing strengths to make further improvements and develop new devices. **Job Qualifications:** + Ph.D. in Material Science, Electrical Engineering, Applied Physics or similar technical field. Emphasis on semiconductor physics or opto-electronic devices preferred. At least 2 years of relevant technical experience. + **Applicants must be either a U.S. citizen, U.S. national, legal permanent resident, asylee, refugee or must be eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce.** + Experience with semiconductor processing - lithography, dry etch, dielectric and metal depositions preferred + Ability to read and understand information and ideas presented in writing + Ability to clearly communicate information and concepts both verbally and in writing + Mathematical Reasoning - the ability to choose the right mathematical methods or formulas to solve a problem. + Inductive Reasoning - the ability to combine pieces of information to form general rules or conclusions (includes finding a relationship among seemingly unrelated events). + Deductive Reasoning - the ability to apply general rules to specific problems to produce answers that make sense. **Salary Range:** $141,900.00-$189,200.000 **Pay Transparency** The anticipated salary range listed for this role is only an estimate. Actual compensation for successful candidates is carefully determined based on several factors including, but not limited to, location, education/training, work experience, key skills, and type of position. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions. Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

We are searching for an experienced Clinical Development Scientist - Strategy to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team. The main responsibilities of the Clinical Development Scientist - Strategy are to determine clinical strategy in conjunction with team members, write clinical protocols, analyze data, and write reports to support the clinical documentation of diagnostic devices in the field of tissue-based, and liquid biopsy cancer diagnostics. This position also engages we external partners, such as clinical research organizations, on areas of governance and strategic partnerships. Further responsibilities include contributing to overall clinical strategy, assist in forecasting/scoping of clinical needs on future/current projects. Additional responsibilities will be to support clinical evidence generation, in conjunction with cross-functional teams as part of the co-development process of companion diagnostics in the field of oncology. This position will support clinical trial study designs and execution, regulatory applications, and scientific marketing deliverables. The ideal candidate will have a strong background in clinical science/research and experience working in pharmaceutical, biomarker, and/or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, Business Development personnel, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory. Responsibilities include but are not limited to: Determine clinical strategy for Agilent's in-vitro diagnostic devices. Scoping and forecasting clinical support of proposed and current projects. Manages and oversees the governance, for internal and external stakeholders (Agilent and external laboratory sties, respectively). Lead clinical strategic initiatives such as scoping and forecasting clinical efforts on upcoming projects and coordinating Medical Affairs and Clinical Affairs publication strategy. Provide thought leadership on key relevant clinical topics to support strategy development and execution. Generation of content to support external validation studies including study design and authoring of study protocols and reports. May also contribute to cutoff/cutpoint determination studies, method comparison, bridging, and analytical concordance studies. Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms. Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials. Ensure scientific validity of reported results including statistical analysis, tabulation, and presentation of data. Collaborate with regulatory and development teams during the submission process including authoring of clinical performance information and other documentation such as Instructions for Use (IFU). Provide clinical and scientific oversight of local marketing and commercial materials. Ensure effective, efficient and compliant Clinical Affairs processes including preparing, revising, and maintaining standard operating procedures for the conduct of clinical studies. Serve as the clinical science subject matter expert in cross-functional internal meetings as well as meetings with pharmaceutical partners and regulatory bodies. Author manuscripts, abstracts, whitepapers and prepare oral/poster presentations. Support audits and inspections as a clinical subject matter expert. Qualifications Master's degree or advanced degree (e.g., Ph.D., Pharm. D., M.D.) in pharmaceutical, medical or relevant biomedical science fields. Advanced Degree preferred. 4+ years of experience in clinical research, medical writing, clinical science in the medical device and/or pharmaceutical industry. Familiarity with clinical trial design, conduct, and oversight including biostatistics, and Good Clinical Practice. Ability to interpret regulatory standards, guidance, and laws. Strong scientific, medical writing, and presentation skills. Exceptional ability to manage multiple projects in a fast-paced environment with changing priorities. Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments. Experience working with external partners and/or regulatory bodies including the FDA. Knowledge in oncology and/or pathology preferred. #LI-PK1 Additional Details This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least April 6, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $100,720.00 - $188,850.00/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 Affirmative Action employer. We value diversity 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 diversity in the workplace 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: Medical/Clinical

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.

Santa Barbara Cottage Hospital seeks a Research Assurance & Integrity Associate responsible for performing complex and confidential duties to facilitate the oversight of research compliance activities, which include legal interpretations of the laws governing human subjects research. This highly organized individual will be expected to work both independently and as a team member to achieve departmental and system wide goals of research integrity. Responsible for Human Subject Protection education and training; monitoring and tracking regulatory requirements related to research on human subjects, specimens, and/or their data; establishing and conducting ongoing auditing and monitoring functions in order to promote investigator research integrity and compliance; and assisting investigators and research team members with interpretive regulatory advice pertaining to their research proposals. QUALIFICATIONS: All job qualifications listed indicate the minimum level necessary to perform this job proficiently. Education: * Minimum: Bachelor's Degree with emphasis in Research Ethics, Law, Policy, Public Health, or Regulatory Compliance, etc. * Preferred: Graduate level education in any of the above. Certifications, Licenses, Registrations: * Minimum: Certified in Healthcare Research Compliance (CHRC) within three (3) years of hire. * Preferred: Association of Clinical Research Professionals - Certified Professional (ACRP-CP); Certified IRB Professional (CIP); Certified in Healthcare Research Compliance (CHRC). Technical Requirements: * Minimum: Working knowledge of scientific and medical concepts and terminology. Excellent communication and writing skills. General office equipment and computer skills, including MS Office. Years of Related Work Experience: * Minimum: 3 years of experience working with legal interpretation of laws governing healthcare or human subject research. This experience may have been gained through employment, internship, or post-graduate education. * Preferred: 1 year in a position which requires regulatory analysis, interpretation, and enforcement. Experience in a legal environment is a plus. Direct experience with regulations involving human subjects research.

The Scientist, Process Development, is a critical position responsible for development activities associated with cell therapy process development and design at Fujifilm Diosynth Biotechnologies, California (FDBC). This position provides hands-on support for all aspects of process development experimental design and execution, will be responsible for experimental process monitoring (data capturing), and process troubleshooting. This position will work closely with and/or under the direction of a Senior or Principal Process Development Scientist. Company Overview At FUJIFILM Diosynth Biotechnologies California, we're driving the future of medicine with the expertise to produce life-changing cell therapies like T-cell and CAR T immunotherapies. Working with pioneering biotech partners, our teams manufacture innovative treatments that improve lives. Join us at our advanced Thousand Oaks facility, where you'll make a tangible impact on groundbreaking therapies. We offer a collaborative, flexible workplace and a vibrant culture driven by passion and energy-what we call Genki. If you're ready to reimagine the future of healthcare, let's create something extraordinary together. Our campus is in Thousand Oaks, California, an exceptional place to live with great schools, natural beauty, outdoor activities, and proximity to Los Angeles and Santa Barbara. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Reports to: Senior Scientist/Principal Scientist, Manufacturing Science and Technology Location: Thousand Oaks (northwest Los Angeles), CA Travel: Travel required (up to 10%) Primary Responsibilities: Support instrument qualifications and change assessments Author and review laboratory procedures, development reports, qualification protocols/reports, risk assessments, standardized unit operations modules, and technical reports Train Process Engineering and Manufacturing staff members on new processes or process changes Supports technology transfer related activities for NPI and implementation of process changes into manufacturing from a technical, development perspective. Partners with Process Engineering and NPI teams to identify and drive process optimization initiatives and addresses opportunities for efficiency and capacity improvements in all areas of internal and external manufacturing and works with team to communicate out to client. Evaluates and provides input to Process Sciences and clients on suitability of technologies, scalability, and manufacturability during process development activities and partners with for defining the critical process parameters of new processes. Physical Demands: Subject to extended periods of sitting and/or standing, vision to monitor and moderate noise levels. Work is generally performed in an office, manufacturing plant, or clinical environment. Car and airplane (see above) travel is an essential part of the job. Qualifications: Bachelor of Science (B.Sc.) with 5+ years of experience or an equivalent combination of education; or Master of Science (M.Sc.) with 3+ years of experience; or PhD in Science with 1+ years of experience or Associate degree with 6+ years of experience; or High School Diploma with 7+ years of experience Proven ability to work with high performing teams. Ability to organize, structure work in a changing environment. Strong technical analysis, business judgment and clear decision-making. Excellent interpersonal skills, interact with, influence, resolve conflict and drive consensus among individuals from a variety of cultures, and disciplines. Demonstrated experience supporting technology transfers, cGMP manufacturing operations and CMC regulatory submissions and inspections required. Advanced knowledge in cell biology, cell culture, cell processing and cell cryopreservation principles. Advanced knowledge across cell culture technologies, cell processing technologies, cell characterization methods, manufacturing under cGMP, validation, Quality Systems, and regulatory requirements. Demonstrated in-depth skills in designing, executing, and interpreting experiments. Strong communication skills (e.g., clear, and concise), team player, and proven negotiation skills. Good decision-making with strong judgment through collaboration and consideration of others point-of-view. Self-motivated, flexible, and creative leader, able to prioritize, multi-task, and work in a fast-paced & demanding environment. Flexibility to travel as required to accommodate business needs Expert problem-solving skills. Effective interpersonal skills as a team player. Role model for FDBC values of trust, delighting our customers, Gemba, and Genki. Salary and Benefits: $104,000 to $130,000, depending on experience Medical, Dental and Vision Life Insurance 401k Paid Time Off To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. *#LI-Onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

Ideal candidate: Recent PHD graduate or a M.S. 3-4 YOE. Technical skills: Recent cell culture experience, plate based assays, imaging experience, flow cytometry. Basic research project experience. Scientist who supports our Emerging Modalities group. In this interdisciplinary role, you will join a fast-paced, cross-functional product team focused on discovering new treatment strategies for human diseases. Routinely culture and manipulate workhorse cell lines with the highest cell culture etiquette Support ongoing early-stage discovery projects by developing appropriate cell-based assays for hit validation and mechanism of action studies. Develop and perform cell-based complementation assays such as split systems (Bimolecular Fluorescence Complementation (BiFC) and Bimolecular Luminescence Complementation (BiLC)) and Co-immunoprecipitation assays as needed by the projects. Basic Qualifications: PhD degree in cell and molecular biology, biochemistry, or a related field with applicable training/experience as demonstrated by recent jobs/publication records Preferred Qualifications: Hands-on experience in mammalian cell culture, cell-based functional assay, transfection, transduction, cell engineering, flow cytometry, western, qPCR, MSD, high-throughput screening, or similar biochemical assays or cell and molecular biology techniques Prior knowledge and experience in supporting projects that involve sample preparation for FACS, FACS data collection and analysis, antibody staining, immunofluorescence, and confocal microscopy can also be highly valuable. Be highly proficient in planning and conducting day-to-day experiments to generate high-standard data and analyze them as needed to create reports for broader team sharing and keep detailed records of all activities on time. Self-motivated to drive the project tasks and troubleshoot them without frequent guidance Strong written, verbal, and oral communication skills and be a team player Top 3 Must Have Skill Sets: M.S or PHD Recent cell culture experience, plate based assays, imaging experience, flow cytometry. Basic research project experience. Pay Rate between $37 - $42 on W2 based on experience. "This posting is for Contingent Worker, not an FTE"

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)

As a Recruitment Research Associate, you will be a key member of a small, high performing search team. We're looking for people who are deeply curious and committed to completing difficult assignments, fueled by connecting with others, an intense hunger to learn, a passion for service, generosity, and a global perspective. We view recruiting on behalf of our clients as a privilege and as ambassadors of their brand. This is a part-time role. What You'll Tackle: Research and Candidate Identification Develop a deep understanding of the various roles we are recruiting for. Implement a search strategy by performing extensive research relevant to each individual search using firm resources Compile data on candidates into firm database. Matching strategic objectives of a role to the experience of a prospective candidate Candidate Outreach Proactively initiate contact with relevant potential candidates and sources through persistence and diligent follow up in order to quickly develop optimal candidates for each search and bench position using various resources and communication methods. Build relationships with prospective candidates through high touch customer service, proposing appropriate candidate opportunities in alignment with candidate careers, leading to a positive candidate experience. Maintain ongoing relationships through regular marketing campaigns with targeted talent segments, leading to the development of talent pools and talent pipelines eventually creating a sustainable talent supply chain. Marketing Write and edit compelling job description copy. Manage job postings. Communicate open roles through various firm social media marketing channels. What's Needed to Win Bachelor's Degree (or in progress). 1+ years' experience and success in an administrative support or research role in an entrepreneurial environment. Persistence, creativity, and resourcefulness. Excellent communication skills (written and verbal). Advanced skills in internet and social media research. Highly organized and detail-oriented Proven team player with experience as an effective member of a close-knit team Compensation Hourly base in addition to performance/activity-based incentives About Our Firm The Brett Fisher Group is a boutique, recruiting firm specializing in confidential, off-market searches, placing exceptional talent in management and director level roles in accounting, finance, sales, and marketing, in clients throughout greater Los Angeles and across the U.S. Learn more at BrettFisherGroup.com and ******************************************** We transform lives of the people we work with, connecting professionals with opportunities that allow them to achieve happiness and career fulfillment. We thrive on hearing people's stories and learning about what excites them about their career, their hopes and their aspirations. By connecting these inspired individuals with our forward-thinking clients, both parties grow and prosper in ways that neither had imagined. We are about dreaming big, and making it happen, and aligning ourselves with people who are up for the same. Interviewing immediately.

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

The Scientist, Process Development, is a critical position responsible for development activities associated with cell therapy process development and design at Fujifilm Diosynth Biotechnologies, California (FDBC). This position provides hands-on support for all aspects of process development experimental design and execution, will be responsible for experimental process monitoring (data capturing), and process troubleshooting. This position will work closely with and/or under the direction of a Senior or Principal Process Development Scientist. Company Overview At FUJIFILM Diosynth Biotechnologies California, we're driving the future of medicine with the expertise to produce life-changing cell therapies like T-cell and CAR T immunotherapies. Working with pioneering biotech partners, our teams manufacture innovative treatments that improve lives. Join us at our advanced Thousand Oaks facility, where you'll make a tangible impact on groundbreaking therapies. We offer a collaborative, flexible workplace and a vibrant culture driven by passion and energy-what we call Genki. If you're ready to reimagine the future of healthcare, let's create something extraordinary together. Our campus is in Thousand Oaks, California, an exceptional place to live with great schools, natural beauty, outdoor activities, and proximity to Los Angeles and Santa Barbara. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Reports to: Senior Scientist/Principal Scientist, Manufacturing Science and Technology Location: Thousand Oaks (northwest Los Angeles), CA Travel: Travel required (up to 10%) Primary Responsibilities: * Support instrument qualifications and change assessments * Author and review laboratory procedures, development reports, qualification protocols/reports, risk assessments, standardized unit operations modules, and technical reports * Train Process Engineering and Manufacturing staff members on new processes or process changes * Supports technology transfer related activities for NPI and implementation of process changes into manufacturing from a technical, development perspective. * Partners with Process Engineering and NPI teams to identify and drive process optimization initiatives and addresses opportunities for efficiency and capacity improvements in all areas of internal and external manufacturing and works with team to communicate out to client. * Evaluates and provides input to Process Sciences and clients on suitability of technologies, scalability, and manufacturability during process development activities and partners with for defining the critical process parameters of new processes. Physical Demands: * Subject to extended periods of sitting and/or standing, vision to monitor and moderate noise levels. * Work is generally performed in an office, manufacturing plant, or clinical environment. Car and airplane (see above) travel is an essential part of the job. Qualifications: * Bachelor of Science (B.Sc.) with 5+ years of experience or an equivalent combination of education; or Master of Science (M.Sc.) with 3+ years of experience; or PhD in Science with 1+ years of experience or Associate degree with 6+ years of experience; or High School Diploma with 7+ years of experience * Proven ability to work with high performing teams. * Ability to organize, structure work in a changing environment. * Strong technical analysis, business judgment and clear decision-making. * Excellent interpersonal skills, interact with, influence, resolve conflict and drive consensus among individuals from a variety of cultures, and disciplines. * Demonstrated experience supporting technology transfers, cGMP manufacturing operations and CMC regulatory submissions and inspections required. * Advanced knowledge in cell biology, cell culture, cell processing and cell cryopreservation principles. * Advanced knowledge across cell culture technologies, cell processing technologies, cell characterization methods, manufacturing under cGMP, validation, Quality Systems, and regulatory requirements. * Demonstrated in-depth skills in designing, executing, and interpreting experiments. * Strong communication skills (e.g., clear, and concise), team player, and proven negotiation skills. * Good decision-making with strong judgment through collaboration and consideration of others point-of-view. * Self-motivated, flexible, and creative leader, able to prioritize, multi-task, and work in a fast-paced & demanding environment. * Flexibility to travel as required to accommodate business needs * Expert problem-solving skills. * Effective interpersonal skills as a team player. * Role model for FDBC values of trust, delighting our customers, Gemba, and Genki. Salary and Benefits: * $104,000 to $130,000, depending on experience * Medical, Dental and Vision * Life Insurance * 401k * Paid Time Off To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. * #LI-Onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

Interested in breaking into biotech drug development? Integrity Bio is a great place to take your university lab experience and learn cutting edge industry skills. Integrity Bio, Inc. specializes in biologics formulation development and drug product manufacturing. We have formulated over 200 biologics including vaccines, antibodies, proteins, and peptides for more than 150 firms. Integrity Bio specializes in hard-to-formulate products in liquid and lyophilized forms. We are located in Camarillo and Thousand Oaks California, the center of a highly concentrated cluster of 10,000 biotech professionals. Demand for our research services increased by 30% in the past year, driving continued expansion and need for great people. We are seeking candidates for the position of Research Associate I or II in Research and Development . Job Description and Duties: Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Set up and perform HPLC, as well as other assays, to characterize protein and peptide molecules. Analyzes, records, and reports the results and conclusions for laboratory experiments. Summarizes and interprets data. Designs protocols and procedures with supervisor. Participates and contributes at group and project meetings as required. Attends and presents at internal and consumer conferences as required. Provide guidance and support to other research associates and lab technicians. The candidate will work well independently and with different functional groups. The candidate should also be open to learn new laboratory techniques and work under the guidance of experienced researchers. The successful research associate will also have the proven ability to manage, multitask and maintain flexibility to changes in a given study. Knowledge of good documentation practices and keeping laboratory notebooks up to date with operations performed in the lab Requirements Qualifications: We are seeking an individual that is pro-active, goal-orientated, and possesses strong organizational and documentation skills. Good interpersonal and proven communication skills, both written and oral, are required. The ideal research associate will possess a Bachelor's degree in biochemistry, analytical chemistry, biological sciences, or related and have 1-5 years of pharmaceutical / biotech laboratory experience. Experience: Having a working knowledge of various analytical and laboratory techniques such as HPLC, spectrophotometry and SDS-PAGE are highly desired. Familiarity with pH analysis, gel electrophoresis, UV/Vis analysis, and various wet chemistry techniques. Understanding of DSC, lyophilization, and Karl Fisher analysis is a definite plus. Experience with Word, Excel and Power Point is required. No relocation assistance will be provided. Integrity Bio Incorporated is an EEO employer - M/F/Vets/Disabled View all jobs at this company

Responsibilities include * Uplift the mission and goals of Aventura Math Camp in all interactions and activities * Engagement in training activities * With guidance from AMC STEM Teachers, preparing for, leading, and co-leading classroom activities * Interacting with and guiding campers during non-classroom activities * Accompanying campers to and from camp via the camp bus at least one day per week * Communication with and guidance of camp visitors The Scholars must be available full-time during the following periods: June 23 - 27: Camp staff training and final camp preparation Hours: 9 am to 5 pm Mon - Thursday June 23 - 26 Hours: 9 am to 7 pm Friday (evening gathering for campers' families) July 7 - 31: Aventura Math Camp, 8 am to 4 pm Monday - Thursday (Fridays off) Aug 1: Break-down/ pack-up/ assessment, 9 am to 5 pm REQUIREMENTS OF POSITION: Required Qualifications * Junior, senior, or teaching credential student standing * Intent to pursue a teaching career * Majoring in a STEM field or pursuing a secondary teaching credential in STEM * Proficiency with standard computer applications * Excellent organizational and communication skills * Ability to demonstrate good judgement and work independently * Ability to perform as part of a team * Basic proficiency with the mathematical ideas corresponding to the California K12 standards Preferred Qualifications * Working knowledge of the Spanish language * Familiarity with any Indigenous Mexican language * Interest in or experience with K12 outreach while a university or college student A background check (including a criminal records check) must be completed satisfactorily before any candidate can be offered a position with the CSU. Failure to satisfactorily complete the background check may affect the application status of applicants or continued employment of current CSU employees who apply for the position. The person holding this position is considered a 'mandated reporter' under the California Child Abuse and Neglect Reporting Act and is required to comply with the requirements set forth in CSU Executive Order 1083 Revised July 21, 2017 as a condition of employment. Hiring Salary: Up to $20.00 per hour Advertised: Apr 30 2025 Pacific Daylight Time Applications close: