Scientist Jobs in Lomita, CA

Job Purpose Support product development projects from concept through commercialization, with limited supervision. As part of a team, assist with developing and testing formulas and processes for new products, quality improvements, and cost reductions. Essential Functions Plan and execute experiments using established laboratory/pilot plant/operations methods, ensuring all experiments meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data analysis Interpret experiment results and translate them into possible solutions Execute pilot lab runs, consumer tests, plant trials, and validation trials Lead small and medium projects, demonstrating good teamwork, effectively managing time, and delivering projects on time and in full Maintain ingredient inventory and lot code tracking Work with internal resources to quickly communicate needed information for recalls Safely operate, clean, and maintain labware and equipment used for testing, adhering to sanitation requirements in the handling and preparation of food products Write product, ingredient, and process specifications Develop strong cross-functional relationships within the R&D team as well as with Marketing, Insights, Quality, Operations, Engineering, Regulatory, etc. Bring innovative ideas to support strategic plans and enable R&D to apply this knowledge to assigned projects Collaborate with R&D Supervisor/Manager to develop contingency plans Support food safety program, quality standards, and legality of products manufactured in the facility Perform other job-related duties as assigned Qualifications (Education, Experience, Competencies) Bachelor's degree in food science or related field 2-4 years of R&D product development experience in the food and/or beverage industry Knowledge of food ingredient functionality, product formulations, and modification techniques Knowledge of all stages of the product development life cycle and product development methodologies Understanding of manufacturing equipment, their processes, and capabilities Strong passion for science, creative thinking, and product development Good cross-functional and peer relationship building skills Proficient computer skills including Microsoft Office programs: Outlook, Word, Excel, PowerPoint Strong written, verbal, and interpersonal communication skills Detail oriented with strong problem-solving and analytical skills Self-motivated with the ability to work independently, organize and prioritize, show flexibility, and multi-task to execute simultaneous projects and activities to meet objectives and deadlines Ability to thrive in a fast-moving and constantly evolving high-growth environment California, Colorado, Connecticut, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, Nevada, New Jersey, New York, Rhode Island, Vermont, Washington, Washington, D.C. Residents Only: The salary range for this role is $58,839 to $73,549 annually. Pay is based upon several factors including but not limited to local labor markets, education, work experience, certifications, etc. Rise Baking Company complies with all minimum wage laws as applicable. In addition to your annual salary, Rise Baking Company offers benefits such as a comprehensive benefits package, annual bonus eligibility, incentive and recognition programs and 401k contributions (all benefits are subject to eligibility requirements). At Rise Baking Company, our people are our finest ingredient. MON123 RISE123 Compensation details: 68640-80000 Yearly Salary PIfc15c1674164-26***********6

Clear Skies is incubating a stealth venture that uses an AI-powered platform to serve major stakeholders in private equity. We operate at the intersection of finance/AI to optimize deal flow, automate decisioning, and integrate networks into a seamless customer journey. Our team is composed of seasoned professionals from private equity, financial advisory, human capital, and AI engineering. We are seeking a Founding Head of AI Products to spearhead the development of AI-driven solutions that redefine how investments are sourced, evaluated, and executed. You will define the product and lead AI initiatives to solve real-world problems in a multi-billion-dollar industry. Key Responsibilities: Product Strategy Execute AI product strategies for market fit and business impact. Analyze customer needs and competitive landscape to uncover new product opportunities. Build business cases with market analysis, ROI projections, and scalability assessments. AI Product Development Define features and workflows to gather customer feedback and iterate on MVP development. Build AI-powered engines to transform large-scale unstructured data into actionable intelligence. Implement NLP techniques for semantic search and keyword matching from unstructured data. Utilize embedding models for vector-based search and context understanding. Workflow Automation Establish scalable AWS-based infrastructure and data pipelines. Develop automated communications, scheduling, and self-service AI tools. Implement best practices for AI model versioning, monitoring, and optimization. Leadership & Collaboration Lead and mentor AI and product teams, promoting innovation and learning. Collaborate with business leaders to align AI strategies with goals. Define and track KPIs to measure product success and guide development. Key Qualifications: 10+ years in product leadership with focus on AI/ML platforms and generative AI technologies. Expertise in AI/ML frameworks (TensorFlow, PyTorch, etc.) and cloud infrastructure. Experience in financial services or private equity is a plus. Application Process: Interested candidates are invited to submit their CV and cover letter detailing relevant experience and qualifications to ***************************. About Clear Skies: Clear Skies is a private equity investment firm that acquires middle-market businesses. We partner with management teams to drive growth and value through our global networks.

Sr. Research Scientist or Research Scientist- Protein Chemistry Kelly Science & Clinical is seeking a (Sr.) Research Scientist for a full-time, on-site, direct hire position at Biotech company in Irvine, CA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Overview We are seeking a (Sr.) Research Scientist to lead R&D efforts in developing reagents and assays to support new biomarker and IVD capabilities. This role will focus on allergen characterization, extraction, purification, and conjugation, as well as the development of allergy-specific IgE, IgG4, and autoimmunity IgG assays (ANA, RF, ds DNA, vasculitis, neuro disorders). The ideal candidate will have expertise in protein stability, SDS-PAGE, Western blot, Abby, and FPLC, with a strong background in protein characterization and assay development. Key Responsibilities Develop reagents for new biomarker and IVD assays, including allergens and autoimmunity assays. Design and execute experiments, analyze data, and interpret results using statistical tools. Lead cross-functional teams to ensure research aligns with product development goals. Collaborate with suppliers to synthesize and characterize custom reagents. Troubleshoot technical challenges and ensure work complies with relevant standards. Oversee the transfer of reagents from R&D to manufacturing with appropriate QC procedures. Mentor research associates and contribute to the training of team members. Qualifications Ph.D. or MS in Chemical Engineering, Biochemistry, Bioengineering, or a related field. 1-3 years of experience in IVD R&D for PhD; 8+ years for MS. Experience with allergen extraction, purification, and conjugation, as well as allergy-specific and autoimmunity IgG assays. Proficient in protein characterization (SDS-PAGE, Western blot, HPLC, FPLC) and purification techniques (IEX, SEC, affinity chromatography). Experience with immunoassay techniques is a plus. Strong background in experimental design, data analysis, and troubleshooting. Excellent communication and collaboration skills. Preferred Skills Bio-conjugation experience, particularly with proteins, peptides, and nucleic acids. Experience developing life science reagents and working in an aseptic lab environment. What Happens Next: Once you apply, our team will review your qualifications. If your skills align with the role, we'll contact you for the next steps in the interview process. Even if this position isn't the perfect fit, joining our network opens the door to future opportunities. We look forward to reviewing your application!

Metric Bio has partnered with a company focused on large-scale carbon removal technologies. This pioneering venture seeks a Senior Scientist in Ocean Modeling to harness electrochemical concepts and proven innovations from top academic research for global, gigaton-scalable carbon dioxide (CO2) removal solutions through direct ocean capture. Using only renewable electricity and seawater, the technology involves no byproducts, and CO2-depleted seawater is returned to the ocean, promoting further atmospheric CO2 absorption. As the Senior Scientist in Ocean Modeling, you will collaborate closely with the Principal Oceanographer and the Monitoring, Reporting, and Verification (MRV) team to validate this breakthrough technology. Key Responsibilities: Lead the company's modeling initiatives, focusing on fluid dynamics and transport in coastal and open-ocean systems. Utilize regional ocean biogeochemical models to assess atmospheric CO2 drawdown and its impacts on ecosystems. Develop and apply near-field fluid dynamics modeling techniques to monitor and forecast plume behavior. Ensure model accuracy and reliability by comparing them against in situ monitoring data. Enhance modeling tools to aid in selecting deployment sites and designing monitoring plans for future expansions. Engage with the marine carbon dioxide removal MRV modeling community to exchange knowledge, share best practices, and incorporate new methods. Work alongside internal MRV teams to ensure modeling efforts align with project goals and organizational objectives. Requirements: PhD in Physical or Chemical Oceanography, or a closely related field. Over 5 years of experience with the Regional Ocean Modeling System (ROMS) or similar frameworks. Expertise in fluid dynamics, seawater carbonate chemistry, and coastal ocean processes. Proficiency in programming languages such as Python or Julia. Strong analytical and problem-solving abilities, with a history of proactive initiative in team settings. Excellent communication skills to articulate complex modeling outcomes to a variety of audiences. A dedicated innovator with a commitment to advancing scalable carbon removal technologies.

Are you excited by the potential of large-scale carbon removal? If so, Captura Corp. is seeking a Senior Scientist in Ocean Modeling to join us. Captura is an early-stage technology start-up with the mission to develop globally scalable carbon removal to support a sustainable future for the world's climate. Captura's unique technology was developed and proven in Caltech's laboratories and uses established electrochemical concepts to enable gigaton-scalable solutions for removing carbon dioxide (CO2) from the atmosphere via direct ocean capture. We capture carbon dioxide using only renewable electricity and seawater, creating no byproducts. CO2-depleted seawater is returned to the ocean to absorb CO2 that comes from the atmosphere. As Senior Scientist in Ocean Modeling, you will work closely with Captura's Principal Oceanographer and the MRV team. This role is critical in the validation of Captura's technology. Key Responsibilities: Lead Captura's modeling initiatives with a strong focus on fluid dynamics and transport in coastal and open-ocean systems. Employ regional ocean biogeochemical models to quantify atmospheric CO₂ drawdown and evaluate ecosystem impacts. Develop and implement near-field fluid dynamics modeling techniques to track and predict plume behavior. Validate models through comparison with in situ monitoring data, ensuring accuracy and reliability. Create and refine modeling tools to support deployment site selection and the design of monitoring plans for future projects. Collaborate with the marine carbon dioxide removal MRV modeling community to share insights, best practices, and integrate new methodologies. Partner with internal MRV teams to align modeling efforts with project goals, timelines, and broader organizational objectives. Educational/Experience Requirements: PhD in Physical or Chemical Oceanography or a closely related discipline. 5+ years of experience utilizing the Regional Ocean Modeling System (ROMS) or similar ocean modeling frameworks. Deep expertise in fluid dynamics, seawater carbonate chemistry, and coastal ocean processes. Demonstrated proficiency in Python, Julia, or other relevant programming languages. Strong analytical and problem-solving skills, with a proven track record of taking initiative and thriving in a collaborative team environment. Excellent communication skills, both written and verbal, to convey complex modeling results to diverse audiences. A passion for innovation and commitment to advancing carbon removal technology at scale.

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 - Cardiometabolic DisordersWhat you will do Let's do this. Let's change the world. We are building upon our solid Cardiovascular foundation and long-term dedication to patients by developing a whole new class of novel molecules, and we need top talent to ensure these molecules become medicines and realize their potential for helping patients. 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, 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 Masters degree and 5 years of scientific experience Or Bachelors 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. #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

Atoco, Inc. is a startup company founded by the distinguished scientist Prof. Omar Yaghi, the inventor of MOF and COF chemistry. Atoco is currently working on technologies in the fields of atmospheric water harvesting and CO2 capture. This position will join the initial startup team that will be working on commercialization of technologies from the University of California, Berkeley. This position will focus on the design and scale up of systems that improve their overall performance in adsorbing/desorbing water vapor. Roles and Responsibilities Work with and report to the head of Product Engineering to achieve the department goals of scaling up commercial-grade MOF/COF-based atmospheric water harvesting technology. Collaborate closely with R&D scientists to process the technical and functional specifications of MOF/COFs coming out of the R&D. Responsible for the system-level design and development of the heat management system, including optimization of heat exchangers, thermal storage, optimization of fluids transfer, pumps, fans, and filters that will operate on the MOF/COFs. Design, plan and scale up the technologies from prototype stage to commercial stage. Identify and optimize critical component and system-level parameters to improve overall product performance in terms of production capacity, energy efficiency, lifetime (reliability/durability), yield, cost, safety, and operation. Evaluate and manage sourcing of materials and components, taking into consideration the whole process from sourcing to final assembly and packaging. Help set up the QC/QA processes and procedures for production. Maintain an electronic notebook detailing all observations and measurements. Contribute to the intellectual property of the company by writing and participating in invention disclosures. Perform periodic reporting to management and participate in technical meetings. Qualifications PhD in mechanical engineering or similar field from an accredited institution, along with a demonstrated record of achievement in research. Strong understanding of thermodynamics, fluid mechanics, and heat transfer. More than 5 years of industrial R&D experience. Industry experience in designing system-level prototypes. Experience in simulation tools for thermal design, thermal analysis, and energy performance Familiar with health and safety procedures in production. Thrive in a culture that values diversity, collaboration, precision, and learning. Strong teamwork and collaboration skills. Excellent problem-solving skills. A track record of successful scale-up prototypes or experimentation. Effective written and verbal communication skills.

Power Brands is the leading beverage development company in North America, with over 3,000 brands developed across categories including energy drinks, functional wellness beverages, plant-based milks, nootropics, hydration formulas, and beyond. We specialize in helping both Fortune 500 companies and high-growth startups bring best-in-class beverages to market - from the first formulation to full commercial production and distribution. ⸻ The Role We're seeking a Senior Beverage Scientist with deep technical expertise in beverage formulation and scale-up. You'll work cross-functionally with our internal team of marketers, designers, and regulatory experts, and directly with clients to develop beverage formulations that meet demanding criteria for taste, function, nutrition, cost, and manufacturability. ⸻ Key Responsibilities • Formulation Development: • Design and optimize beverage formulations across multiple categories: RTDs, energy drinks, plant-based, functional waters, juices, and protein shakes • Select appropriate functional ingredients, sweeteners, stabilizers, acidifiers, preservatives, colors, and flavors • Ensure ingredient compatibility, stability, and regulatory compliance (USDA, FDA, NSF, etc.) • Analytical & Technical Support: • Conduct bench-top trials, Brix and pH testing, shelf-life evaluations, sensory panels, and microbiological assessments • Work with QA to troubleshoot stability, separation, sedimentation, or microbial issues • Manage formulation records and technical documentation for each project • Scale-Up & Production: • Oversee transition from lab to pilot and full-scale production • Interface with copackers and manufacturing facilities to support batching, processing (hot fill, tunnel pasteurization, UHT, etc.), and packaging • Travel as needed to support commercial runs and line trials ⸻ Required Qualifications • B.S. or M.S. in Food Science, Chemistry, Biochemistry, or a related field • 5-10 years experience formulating commercial beverages from scratch, preferably in a consulting, contract manufacturing, or CPG environment • Advanced understanding of ingredient interactions, beverage chemistry, emulsions, pH stability, and processing methods • Experience with shelf-life extension strategies, natural preservatives, clean label ingredients, and nutritional claims • Proficient with formulation software (e.g. Genesis R&D, NutraCoster), lab equipment, and standard operating procedures • Excellent written and verbal communication skills • Self-starter who thrives in a high-growth, high-demand environment ⸻ Absolutely - here's the updated version with your changes included: Preferred Experience • Experience with a wide range of beverage processing methods, including carbonation, pasteurization, aseptic, UHT, hot fill, cold fill, and shelf-stable production • Familiarity with functional ingredients and beverage types across the industry, including tea, coffee, energy drinks, sports nutrition products, adaptogens, nootropics, and ready-to-drink alcoholic beverages • Strong understanding of regulatory requirements, including GRAS status, FDA labeling guidelines, and compliance with Supplement Facts and Nutrition Facts panels • Well-versed in multiple beverage formats and categories, including carbonated, non-carbonated, still, sparkling, powdered, concentrate, and ready-to-drink (RTD) products ⸻ Why Join Power Brands? • Work on groundbreaking products from idea to execution • Exposure to the biggest trends and most exciting innovations in the beverage industry • Collaborate with top-tier talent across formulation, branding, marketing, and operations • Competitive salary, health benefits, PTO, and bonus opportunities • Four day work week optional • State-of-the-art lab, office, and test kitchen in Los Angeles ⸻ How to Apply Send your resume and a brief summary of your most impressive formulation or product launch to ********************** Or apply directly through LinkedIn

About Burning Rock Dx.: Burning Rock Dx. (NASDAQ:BNR) was foundedin 2014, and it is a leading innovator in next-generation sequencing (NGS) technologies, dedicated to advancing precision medicine, genomics research, and clinical diagnostics. We collaborate with global partners to deliver cutting-edge solutions for complex biological challenges. About the Role: We‘re seeking a highly skilled and motivated Clinical Bioinformatics Scientist to join our CAP-accredited molecular oncology laboratory. The candidate will play a crucial role in analyzing and interpreting Next-Generation Sequencing (NGS) data for cancer diagnostics, ensuring compliance with CLIA/CAP guidelines, and contributing to the development of robust bioinformatics pipelines for somatic and germline variant analysis. Key Responsibilities: Analyze and interpret NGS data for molecular oncology applications, including somatic and germline variant calling, copy number alterations, structural variations, and tumor mutational burden (TMB)/microsatellite instability (MSI) analysis. Develop, optimize, and maintain bioinformatics pipelines for clinical NGS testing, ensuring compliance with CAP, CLIA, and FDA regulatory requirements. Perform variant annotation, curation, and classification using public and proprietary databases (e.g., ClinVar, COSMIC, gnom AD, OncoKB). Support quality control (QC) and quality assurance (QA) activities by identifying and troubleshooting technical and computational issues. Collaborate with molecular pathologists, clinical scientists, and laboratory personnel to ensure accurate variant interpretation and reporting. Stay up to date with emerging bioinformatics tools, guidelines, and best practices for NGS-based oncology testing. Assist in validation and verification of new assays, software updates, and enhancements to bioinformatics workflows. Participate in CAP/CLIA audits, proficiency testing, and regulatory documentation. Maintain and develop Laboratory Information Management Systems (LIMS) to support efficient clinical sample tracking, data management, and workflow automation. Work closely with laboratory staff to ensure seamless LIMS integration with NGS pipelines and other bioinformatics tools. Qualifications: PhD in Bioinformatics, Computational Biology, Genomics, Molecular Biology, or a related field, OR MS with at least 3 years of relevant clinical experience. Strong experience with NGS data analysis in a clinical setting, preferably in molecular oncology. Proficiency in Python, R, Perl, Bash, and Linux-based environments for bioinformatics workflows. Familiarity with NGS analysis tools such as GATK, SAMtools, BCFtools, VarDict, Mutect2, Annovar, VEP, and other variant callers/annotators. Experience working with NGS assay validation, quality control metrics, and regulatory compliance (CAP/CLIA/FDA guidelines). Strong knowledge of human genetics, cancer genomics, and clinical variant interpretation (ACMG/AMP/ASCO guidelines). Ability to work in a collaborative, fast-paced clinical laboratory environment with strong analytical and problem-solving skills. Nice to Have: Prior experience working in a CAP/CLIA-certified clinical laboratory. Knowledge of cloud-based bioinformatics workflows (e.g., AWS, Terra, DNAnexus).Experience with database management, pipeline automation, and high-performance computing (HPC) environments. Understanding of laboratory information management systems (LIMS). Prior involvement in NGS assay development, validation, or FDA submission processes. Benefits & Perks: Competitive salary and performance-based bonuses Comprehensive healthcare, dental, and vision insurance 401(k) retirement plan with company matching Paid time off and flexible work arrangements Professional development and conference opportunities Join us in advancing precision oncology through cutting-edge clinical bioinformatics. Equal Opportunity Statement: It is the policy of Burning Rock Dx. LLC to provide equal employment and advancement opportunities to all colleagues and applicants for employment without regard to race, color, ethnicity, religion, gender, pregnancy/childbirth, age, national origin, sexual orientation, gender identity or expression, disability or perceived disability, genetic information, citizenship, veteran or military status or a person's relationship or association with a protected veteran, including spouses and other family members, marital or domestic partner status, or any other category protected by federal, state and/or local laws. As an equal opportunity employer, Burning Rock Dx LLC is committed to a diverse workforce.

Who we are: 20bloc, Inc. (*************** is an early-stage biopharma company creating breakthrough protein-based drugs to save lives. We are developing a safe and effective hemoglobin-based oxygen carrier for first response, organ preservation and oxygen therapy. We value and encourage innovations through robust information exchange, hard work, and team interaction. We are collaborative. We are intellectual. We are hands-on. Job Title: Protein Scientist (Molecular Biology) Position Overview: We are seeking an experienced Protein Scientist with a background in molecular biology and hands-on experience in genetic engineering and yeast-based expression systems. Key responsibilities: Design, construct and optimize innovative recombinant expression systems with yeast such as Pichia/ komagataella phaffii and Saccharomyces strains to produce high-level expression of target proteins. Characterize genetic and phenotypic engineered strains, and analyze expression levels, post-translational modifications, and product quality. Collaborate with fermentation scientists to integrate molecular biology work with bioprocess development and production scale-up. Identify, qualify and manage CROs and coordinate with partners. Write detailed experimental records, scientific reports and presentations. Requirements: PhD in Molecular Biology, Biotechnology, Genetics, Biochemistry, or a related field 2+ years of industry experience working directly on genetic engineering. Track record in molecular cloning, gene editing, vector design, transformation, strain screening, and optimization of yeast expression systems. Proficiency in analytical methods to assess protein expression and quality, such as ELISA, flow cytometry, or glycan analysis. Strong planning and problem-solving skills and ability to work both independently and collaboratively in a multidisciplinary team. Excellent communication skills, with a proven ability to document research findings and present and interpret complex data and findings concisely and clearly. This is an excellent opportunity for a motivated individual to grow and excel in an early-stage biopharma company to develop a groundbreaking drug that could make an impact to the life of many. This is a full time position on-site in Thousand Oaks, CA. 20bloc is an equal opportunity employer. We offer a comprehensive benefits package which includes: Medical, dental and vision plans 120 hours paid time off (PTO) 12 paid holidays annually 401(k) U.S. retirement savings plan Employee assistance program

Summary: The R&D Formulator develops and optimizes formulations, conducts testing, and ensures accurate documentation. Supports technology transfer, collaborates cross-functionally, and stays updated on industry trends. Maintains lab safety, mentors staff and participates in management meetings. Evaluates raw materials, improves formulations, and oversees special projects as assigned. Essential Duties and Responsibilities Formulation creation (bench mix, formulation sheet, product description sheet, sample measurement, color verification, etc.) Writes and/or reviews procedures, purchase orders, quotes, and specifications needed to support product development activities Develops and/or performs all formulation requirements on new formulas Documents test results, specifications, and final formula procedures in a standard format for inclusion in the master file Participates in the technology transfer from pilot scale to manufacturing Communicates, in a timely fashion, all information regarding formulation, project status, raw material research, results, etc. to all appropriate individuals in Purchasing, Sales, Customer Services, and Quality departments Conducts intellectual searches for technical information through a variety of resources Keeps abreast of current trends, practices, developments, and regulatory changes, which would impact products, procedures, or formulation Ensures the maintenance and/or adherence to good laboratory practices and all safety regulations both in laboratory and manufacturing areas Provides technical knowledge in guiding other assistants/technicians in the R&D Lab Develops and presents to the R&D Manager or Director, R&D matters requiring his/her decision Participates in scheduled Management and Sales meetings in the absence of the R&D Manager/Director Evaluate new and alternative raw materials for functionality and stability Assist in verification studies as required Reformulate to improve existing products as needed Special projects as needed and any other tasks assigned by the R&D Director or Manager. Qualifications/Education/Experience: Minimum Bachelor of Science in Chemistry or related field 2+ years' Experience in R&D, Quality Assurance, Quality Control or Manufacturing is required; nutritional, pharmaceutical or biotechnology experience preferred; Have strong eye for color, finish, and detail Must have proficient math skills; weights and volumes experience a plus Excellent communications (verbal/written) Excellent organizational and multi-tasking skills Proficient with MS Word, Excel, Teams, and Outlook Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts, fumes, or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear.

Formulation Scientist- Simply Biotech Are you looking for a new career opportunity with an exciting biotech company?! Then we've got the right team for you! In this role, you're responsible for the duties listed below. Immediate opening for a Formulation Scientist with a biotech company in Torrance, CA who possesses: Bachelor's degree in chemical engineering, chemistry, food science/technology, or similar 2 years' experience in nutritional supplement industry or similar field (working with dietary supplements, pharmaceutical development, etc.) 1+ year experience in granulation techniques, processing, and property characterization Email resumes to ************************** or call ************ FULL DESCRIPTION : The Formulation Scientist is responsible for the development of new products, enhancement of existing formulations, and resolution of manufacturing challenges. This role involves evaluating new and alternative raw materials, identifying cost-saving opportunities, and ensuring compliance with regulatory standards. The scientist will formulate powders, tablets, capsules, and nutrient premixes tailored to customer specifications while considering application requirements, shelf life, processing conditions, and stability. Additionally, this position will contribute to ingredient assessments and provide internal blending instructions as needed. The selected candidate will be responsible for: Thorough understanding of solid dose product development and manufacturing scale-up. Operational understanding of wet and dry granulations, tablet presses, encapsulation machines, ribbon blenders, and V-blenders. Develop and make lab samples of custom dietary supplement blends. Interpret customer requests into prototypes, such as great-tasting powdered beverages or tablets designed with various properties. Work with R&D teams, Manufacturing, supply chain, etc. on scale-up and transfer of developed formulations to the plant. Provide customers with technical support on dietary supplement formulations. Maintain proper documentation of product development process and results and keep equipment logbooks in accordance with R&D guidelines. Comply with company procedural guidelines, laboratory procedures, and safety programs. The selected candidate will also possess: Bachelor's degree in chemical engineering, chemistry, food science/technology, or similar. 2+ years prior experience in a nutritional supplement industry or similar field. 2+ years working with dietary supplements, pharmaceutical development, or similar. 2+ years' experience in granulation techniques, processing, and property characterization. Ability to formulate nutraceutical and powdered functional food prototypes based on nutritional targets as well as to consumer sensory acceptance. Understanding of GMP manufacturing considerations and requirements. Good interpersonal and presentation skills to share development work within the organization and with customers. Ability to work in a physically challenging environment: lift 25 pounds and move up to 50 pounds when working with bulk ingredients, operate pilot scale equipment. Be authorized to work in the United States Salary Range: $75k-85k/yr For immediate and confidential consideration, please email your resume to ************************** or call ************. More information can be found at *********************

Partnered with a growing biotech startup dedicated to CNS drug delivery. As a Research Associate - In Vivo, you will play a crucial role in preclinical research and early drug development, assessing therapeutic candidates in animal models. Key Responsibilities Design and execute in vivo studies using rodent or other mammalian models. Handle and process blood and tissue samples for biochemical and histological assays. Collaborate with cross-functional teams to advance preclinical studies. Maintain laboratory equipment, generate documentation, and assist in data analysis. Present findings to multidisciplinary discovery teams. Adapt to evolving research needs and support various lab tasks as required. Basic Qualifications B.S. or M.S. in Life Sciences (Biology, Neuroscience, Pharmacology, or related field). Strong understanding of CNS disease biology. Hands-on experience with rodent or mammalian animal models. Skilled in tissue processing and sample handling with attention to precision. Familiarity with biochemical/histological analysis techniques and standard lab equipment. Excellent communication, multitasking, and problem-solving skills. Preferred Qualifications Experience with plate-based assays (e.g., ELISA, RT-qPCR). Knowledge of biologics delivery (antibody, oligonucleotide, peptide) in in vivo studies. Proficiency in animal handling techniques (behavioral experiments, perfusion) and tissue processing (sectioning, imaging). Commitment to a two-year tenure for team consistency and growth.

About the Company PakLab is a leading contract manufacturer specializing in health & beauty and household products. With three decades of professional product development service experience, we are setting a new standard in contract manufacturing. With our innate understanding of product design, development and formulation, as well as manufacturing and packaging mechanics, we work with our clients as a fully integrated strategic partner, creating innovative products from the bottom up. We employ a world-class team of Engineers, Chemists, Microbiologists, Lab Technicians, Designers, and Packaging Specialists who oversee the process from conception to completion. Service is the cornerstone of our corporate culture, and we will devote whatever resources are necessary to ensure a complete understanding of our customers' needs in order to achieve their goals. About the Role The Chemist is responsible for the batching of PakLab and customer formulas. Requires an individual that keeps up-to-date with the latest applications of chemicals and is capable of transferring that knowledge into a functional product. Good Attendance. Able to work any shift and extended hours. Must be detailed oriented with strong clerical and time management skills. Able to follow procedures and instructions. Able to work in fast-paced environment with limited supervision. Must work well with others in a close environment. Typical Duties and Responsibilities Develop new personal care product formulations (e.g., cleansers, creams, lotions, serums, hair products) Modify and optimize existing formulas to improve stability, efficacy, or cost-effectiveness Ensure compatibility between active ingredients, emulsifiers, preservatives, and fragrance systems. Must conduct crash stability on all formulations. Ensure formulations comply with FDA, EU, and other regulatory bodies. Work closely with the process engineering team to scale formulations from lab to production. Collaborate with clients to develop formulations based on their briefs. Reformulate based on client feedback, cost targets and ingredient preferences Interact with vendors to obtain information on raw materials to troubleshoot formulas. Keep up with personal care industry trends, consumer demands, and competitor launches Attend trads shows and meet with suppliers for new technologies Follow GLP/GMP and notebook protocol. Maintain the laboratory in clean organized condition. Assist process engineers in first manufacture of production batches. Adjust simple parameters for manufacture of products (such as pH, viscosity, color, etc…). Performs other duties as assigned. Physical Requirements Ability to lift and pull a minimum of 25 lbs. Requires walking and standing for lengthy periods of time. Requires bending, twisting, pulling, pushing and climbing of ladders and stairs. Capable of climbing steps and retrieving material from shelves. Work Experience and Education Requirements Excellent English written and verbal communication skills. Bachelor's Degree in Chemistry, or related field, is required. Master's Degree or PhD preferred. 3 or more years' experience with cosmetics. Knowledge of computer applications. Pay range and compensation package - 75k-100k yearly salary. Equal Opportunity Statement - PakLab is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.

Sharp Medical Staffing is seeking a travel Clinical Lab Scientist (CLS) for a travel job in Los Angeles, California. Job Description & Requirements Specialty: Clinical Lab Scientist (CLS) Discipline: Allied Health Professional Start Date: 05/05/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours Employment Type: Travel Our client is currently seeking a travel Allied MLT in Los Angeles, California for 5x8 Rotating shifts. The ideal candidate will possess a current California license. You must have at least 3 years of overall experience or at least 1 years of recent experience with MLT. Previous travel experience is strongly preferred. Sharp Medical Staffing Job ID #233772. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Allied - CLS About Sharp Medical Staffing At Sharp Medical Staffing, we set the bar for excellence by providing an elite experience for traveling medical professionals. We are a dedicated staffing agency for Nursing, Cath Lab, Electrophysiology, Interventional Radiology, Rehab Therapy and Allied Health. We also specialize in crisis and rapid response jobs nationwide. Benefits Weekly pay Holiday Pay Guaranteed Hours 401k retirement plan Pet insurance Company provided housing options Sick pay Referral bonus Medical benefits Dental benefits Vision benefits

The ideal candidate will be responsible for turning data into actionable insights by recognizing trends and anomalies in multivariate datasets. In order to use these insights for business improvement, this candidate should feel comfortable using their analysis to tell a story. Responsibilities Conduct fact-based research and analysis Assist with publication of research commentaries and papers Evaluate new and established research sources Prepare materials that summarize data and draw conclusions to support key business discussions Qualifications Bachelor's degree or equivalent experience Expertise with SPSS, Excel, and PowerPoint Previous quantitative and qualitative research experience Molecular Biology: real-time PCR, Sequencing, multiplex endpoint PCR, probe-based hybridization and detection Microbiology: handling BSL-II agents and clinical specimens for nucleic acid extraction Perform and evaluate experiments with guidance from supervisor or from written protocols Qualify and maintain automated systems in collaboration with System Engineers Apply basic statistical techniques for data analysis Must maintain a laboratory note book according to GDP Assisting in maintaining laboratory supplies and equipment May be required to perform other related duties as required and/or assigned BS Degree in biochemistry, microbiology, molecular biology, or related fields with 0-2 years of experience Background in molecular biology, biochemistry, and/or microbiology techniques Must have hands on experience in setting up PCR assays Experience in maintenance and troubleshooting of laboratory instrumentation Ability to execute complex experiments with attention to details Experience with IVD assay development and Design Control process is a plus. Ability to prioritize and execute various tasks Demonstrates a sense of urgency, strong work ethics and a “can do” attitude Is curious, inquisitive, innovative, and strives to improve the status quo Willingness to take on challenges and changes as opportunities Collaborates with others in a team-oriented environment Follows Quality System requirements, safety rules and applicable regulations Embraces and leverages diversity of culture and thought Works in a laboratory environment. Is required to lift up to 20 lbs. May be required to sit or stand for long periods of time while performing duties. Ability to work safely with hazardous chemicals and infectious agents. Willingness to work overtime and flexible schedule as needed is a plus.

PRIDE Health is seeking a local contract Clinical Lab Scientist (CLS) Level I for a local contract job in San Juan Capistrano, California. Job Description & Requirements Specialty: Clinical Lab Scientist (CLS) Discipline: Allied Health Professional Start Date: 04/24/2025 Duration: 26 weeks 40 hours per week Shift: 8 hours, evenings, nights Employment Type: Local Contract Pride Health is hiring a Clinical Laboratory Scientist to support our client's medical facility based in San Juan Capistrano CA 92675. This is a 6 -month assignment with the possibility of a contract-to-hire opportunity and a great way to start working with a top-tier healthcare organization! Job Title: Clinical Laboratory Scientist Location: San Juan Capistrano CA 92675 Pay Range: $50 -$55 per hour Schedule: 3 PM - 1130 PM PST (Sun Mo Tu We Th) Duration: 6 Months + *The salary is determined by an individual's level of experience, as well as any relevant licenses and certifications they may hold. We are hiring a Clinical Laboratory Scientist (CLS) to join our team! In this role, you'll be responsible for performing complex clinical lab tests, maintaining equipment, and ensuring high-quality standards in our laboratory operations. If you're passionate about clinical testing and looking for a dynamic environment, we'd love to hear from you! Key Responsibilities: Perform moderate to highly complex clinical tests, following standard procedures. Prepare reagents, media, and controls; evaluate new reagents and materials. Ensure specimen acceptability and accurately analyze results. Conduct regular equipment maintenance, calibration, and quality control checks. Troubleshoot technical issues and communicate effectively with the team. Supervise and train unlicensed staff, ensuring proper procedures are followed. Stay current with continuing education requirements and professional development. Qualifications: BS in Medical Technology or related field. Current CLS license (California). 0-3 years of lab experience (rate based on experience). Proficiency in Microsoft Office applications; automation skills a plus. Physical Requirements: Ability to lift and carry up to 25 pounds. Good eye-hand coordination, with potential color blindness testing. Pride Global offers eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, , legal support, auto ,home insurance, pet insurance, and employee discounts with preferred vendors. About PRIDE Health PRIDE Health is the minority-owned healthcare recruitment division of Pride Global-an integrated human capital solutions and advisory firm. With our robust and abundant travel nursing and allied health employment options across the U.S., PRIDE Health will allow you to help change the way the world lives and heals as it connects you with the industry's leading healthcare organizations. Pride Global offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors. Benefits Weekly pay Holiday Pay Guaranteed Hours 401k retirement plan Cancelation protection Referral bonus Medical benefits Dental benefits Vision benefits

LanceSoft is seeking a travel Cath Lab Technologist Level II for a travel job in Mission Viejo, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 05/06/2025 Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel Years of experience REQ: 2 First-timers accepted: No 4x10s - call required 8days/mo Certs REQ: BLS, Flouro Permit, CA state license About LanceSoft Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities. Benefits Weekly pay Medical benefits