Senior Scientist Jobs in Farmersville, CA

We are seeking a highly motivated Scientist - Synthetic Immunology to join our team who thrives in a dynamic, fast-paced, and creative environment in Menlo Park, CA. You will work closely with the founding team to generate the foundational science at Enoda and play a critical role in the future direction and culture of the company. The ideal candidate has a broad range of cell engineering experience with a focus on performing cell-based and in vivo assays to develop the next generation of cell and gene therapies. In close collaboration with team members, you will lead the development and optimization of novel tools that convert a plethora of interesting cell types into optimal disease fighting machines. As an early employee, you will have a huge impact on the culture and research of a team dedicated to saving lives through cell engineering. Enoda's Vision Synthetic biology has transformed cells into medicine, harnessing their native potential to target cancers, clear viral infections, repair wounds, overcome autoimmunity, reverse aging, and beyond. At Enoda, we believe that the cells that make up our bodies hold the key to cure everything that afflicts us. Our mission is to chart the phenotypic landscape of our cells, discovering ways to transform them into potent disease fighting machines. The development of cell and gene therapies has been dominated by relying on what is currently known to double down on specific receptors, cell types, and indications without regard for finding the optimal mix. Enoda is a team of synthetic biologists looking to reverse this paradigm by combining our novel receptors that exploit untapped pathways with high-throughput screening and systems immunology - engineering the right cell type with the right tools for the right indication. We are building towards a future where every facet of cells are precisely engineered to maximize the therapeutic potential. Responsibilities Validate and characterize novel molecular tools in clinically relevant cell types (e.g. T cells, NK cells, myeloid cells, stem cells). Conceive, plan, and execute cell-based methodologies to streamline the phenotyping of next generation cell and gene therapies. Translate screen-derived hits into in vivo validated lead cell and gene therapies for drug candidacy. Contribute to the analysis and interpretation of multiple immunological data streams. Collect, organize, and analyze data to guide decision-making processes. Mentor younger scientists and research associates. Influence and support company operations, vision, and culture. Required Qualifications PhD in biology, bioengineering, immunology or equivalent experience. Experience developing and executing cell-based methods to validate and optimize molecular tools (e.g CRISPR, synthetic receptors, or si RNA). Experience planning and coordinating with internal/external teams for in vivo experiments. 5+ years hands-on mammalian cell culture experience. Have a demonstrated record of leading impactful projects. Ability to document and maintain an organized account of lab work and results. Demonstrated ability to identify, troubleshoot, and resolve problems quickly. Excellent communication skills, with the ability to effectively convey complex technical information. This job might be great for you, if you… Want to take on responsibility and lead the development of transformative medicines. Enjoy working in a small team of impact-oriented engineers and scientists. Are an effective multitasker with the ability to advance multiple projects simultaneously. Are passionate about building a community dedicated to helping the world through cell engineering. Have extensive knowledge of immunology and manipulating primary human cells. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA writing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, please apply via LinkedIn. Job Description: Senior Research Assistant / Associate Scientist, Assay Development / Analytical Development Position Overview: The SRA/Associate Scientist in Assay Development and Analytical Development will play a critical role in the development, qualification, and validation of analytical methods to support our RNA editing programs. The successful candidate will work under the guidance of an assay development scientist to develop custom assays for the analysis of samples, including AAVs, cells, and tissues, and will ensure that all methods and processes are in accordance with FDA and ICH guidelines. This role also involves aiding in method transfer and oversight of sample analysis at Contract Research Organizations (CROs), as well as drafting Standard Operating Procedures (SOPs), method development reports, and regulatory documents. Key Responsibilities: Method Development, Qualification, and Validation: Support the development, qualification, and validation of analytical methods in accordance with FDA and ICH guidelines. Ensure robust and reproducible methods for the analysis of AAVs, cells, and tissues. Develop, optimize, and implement analytical methods for the characterization, release, and stability testing of Amber's gene therapy. Sample Analysis: Support drug absorption, distribution, metabolism, and excretion studies. Perform analysis of AAVs, cells, and tissues to support various stages of research and development. Interpret and present analytical data to support decision-making processes. Lead efforts to streamline and optimize sample storage and processing, as well as establishing and maintaining critical reagent stocks and cell banks. Method Transfer and Oversight: Ensure the accuracy and consistency of sample analysis conducted by external partners. Provide technical guidance and support to CROs as needed. Documentation and Reporting: Draft and review SOPs, method development reports, and regulatory documents. Maintain accurate and detailed records of all experiments and analyses. Qualifications: B.A./B.S. or M.S. in Molecular Biology, Biochemistry, Analytical Chemistry, or a related field. 5+ years of experience in assay development and analytical development in the biotechnology or pharmaceutical industry. Experience using automated systems to perform high-throughput RNA extractions. Experience with RNA-based therapies is highly desirable. Familiarization with FDA and ICH guidelines for method development, qualification, and validation. Hands-on experience with analytical techniques such as PCR, qPCR, dd PCR, ELISA, and cell-based assays and detection methods such as fluorescence, luminescence, and ECL. Prior history in compiling and analyzing data and generating reports that are routinely presented to project teams and executive management to enable decision-making. Experience writing transfer test methods and regulatory filings is a plus. Ability to work effectively in a collaborative, fast-paced environment. Preference will be given to those who display: High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. Team-oriented thinking. Demonstrated excellence in small team environments, including a “no task is too small” attitude. If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

Senior Research Associate/ Associate Scientist Upstream PD: Job Description Celltheon is seeking an innovative, independent and motivated professional with 3-5 years of experience and expertise in mammalian expression technologies including cell line development of monoclonal antibodies and other recombinant proteins. The successful candidate will join a team developing recombinant cell lines and upstream manufacturing processes. Requirements include: Cell Line Development: 3+ years of hands-on industry experience with CHO cell line development. An ideal candidate understands cell line development procedures and technologies for transfection, resistance selection, cell counting, clonality documentation, cell passaging, clone selection, clone stability assessment, media adaptation, media and feed preparation, cryopreservation, and process optimization to improve protein expression. Process Development Experience: An ideal candidate has bioreactor operation experience (stir-tank and WAVE bioreactors), developing scalable upstream processes for manufacturing. Data maintenance and interpretation: Collects and compiles data and records in ELN and maintains batch records, ensures they are consistently updated, and well maintained. In addition, the candidate must be able to create and revise existing SOPs, as methods are developed and modified. MINIMUM REQUIREMENTS: BS/MS in Biotechnology, Bioprocessing, Bioscience or a related subject Ideally has 3-5 years of relevant industry experience in CHO upstream PD Good verbal and written communication skills including report writing. ABOUT CELLTHEON: Located in the SF Bay Area, Celltheon Corporation has developed novel mammalian expression technologies which enhance the productivity of recombinant proteins. Celltheon leverages its proprietary platforms to provide custom services to the biotech industry. We are dedicated to offering our clients a diverse range of technical expertise from molecular biology, cell culture, purification process development, and generation of early-stage pre-clinical material. Celltheon employees enjoy the benefit of having the opportunity to work in a diverse challenging and technical environment with a chance to learn and contribute in multiple areas, offering both personal and professional growth in a short time frame. Celltheon seeks talented and dedicated individuals to join its growing team. Celltheon offers a competitive salary and benefits program. If you desire a position in an active, collaborative scientific environment with the opportunity for professional growth and a chance to make a difference, please connect with us on LinkedIn. Our website: ************************

Patco Brands is one of the fastest-growing beverage companies in the United States. Independently owned, Patco has established itself by using 100% Blue Weber Agave and a proprietary process to innovate within the fast-growing ready-to-drink spirits category. Patco Brands is a maker of margaritas, tequila, hard seltzers, Irish cream liqueur, and other spirits under our own brands and for private labels. Our own brands, with nationwide distribution, include: · Rancho La Gloria Ready to Drink Margaritas · Rancho La Gloria Ranch Water · Big Sipz · Kirkland Signature Tequila · Kirkland Signature Hard Seltzers · Dough Ball Whiskey Patco products are sold in every major retailer including Costco, H.E.B., Kroger's, Target, Walmart, and Whole Foods Market, just to name a few. -------------------------------------------------------------------------------------------- Our senior R&D scientist will be in our Sausalito office and will assist in the development of new and current products for formulated wine, beer, and spirit beverage categories. The ideal candidate has an impeccable palate, is highly organized, and has experience working with alcoholic beverage formulation. Responsibilities: Drive new product development processes, including formulation trials, stability testing, and prototype development of RTD cocktails, hard seltzers, wines, and spirits. Work with other departments in supporting new product development Be proactive with the improvement of products Manage and lead projects such as creating technical plans, risk management, and supplier mitigation plans from concept to commercializatio.n Work with flavor and ingredient suppliers (and the internal procurement team) to ensure a steady source of ingredients is available. Stay on top of alcohol trends in industry. Collaborate with Legal on formula filings and ensure compliance with product development. Work with the Executive Team on managing technical timelines for new products and research projects. Assist with preparing sensory samples and compound dilutions and blending for production. Advise on formulation requirements for regulatory and label considerations Coordinate testing for products as required Ensure FDA or TTB requirement activities are compliant Conduct product quality tests, including shelf life and product stability studies Manage lab space and equipment and assist with general lab operation Document all experimental procedures in a laboratory or digital notebook Requirements: BS or higher degree in preferably Food Science/Chemistry or a related discipline 5+ years of experience in consumer product development Experience implementing processes in food and beverage product development Experience managing and developing a team of food scientists Strong knowledge of TTB and/or food and beverage regulatory compliance Passionate about food and beverage, and especially alcohol beverage products Exceptional palate and sensory skills Highly organized Strong communication skills By applying for this position, we are collecting personal information from you. Please read our privacy notice in the link below for information on how we collect and process your personal information. *******************************************

Position Type: Full-Time Compensation: Annual salary $80,000 - $90,000 and performance-based bonuses Nexture Bio is seeking a skilled and motivated Biomaterials Scientist to help drive the development of advanced biomaterials to enable the field of cell-cultured meat and support the development and implementation of a scale-up strategy for materials production. This full-time in-person position in Vacaville, CA will work in a GMP facility where you will support R&D and production. The ideal candidate will be a technical expert and have hands-on experience with the forming of biopolymers through various methods (e.g., electrospinning equipment and/or various shaping, spraying, and fiber spinning or extruding techniques) contributing to innovative product development and process optimization. Additionally, this role will work with external partners to investigate scale-up manufacturing methods and tech transfer existing formulations to these new methods. This role reports directly to the VP of Research & Development. Nexture Bio develops animal-component-free microcarriers, scaffolds, and cell-attachment factors made with ingredients that are safe and suitable for use in food products. Nexture Bio is a Generation Food Rural Partners (GFRP) portfolio company, launched in December 2023. Key Responsibilities: Design, develop, and scale up biomaterial products for mass production. Lead internal pilot-scale production and tech transfer for biomaterial products. Operate and maintain equipment for experimental and production activities. Collaborate with cross-functional teams, including tissue engineers, product developers, and R&D staff. Occasional travel may be required; approximately 10% time. Document research findings, methods, and production techniques, ensuring traceability and reproducibility. Stay up-to-date with industry advancements and integrate new technologies into Nexture Bio's processes. Advise the management team on product and patent development and present work to peers, reviewers, conferences, and customers Provide customer support and service. Troubleshooting upstream and downstream equipment operations. Maintain and execute the Preventive Maintenance Program and offer process improvements. Leading training initiatives on reliability improvements, ensuring operators are up to date and compliant on new processes. Support a dynamic operations team and build systems with them. Lead project efforts to support company-wide goals to scale the cultivated meat industry. Commission and validate new equipment. Be ready to thrive in a startup environment by taking on any task as needed. Skills and Qualifications: Background in Materials Science, Chemical Engineering, Chemistry, or a related field. Bachelor's degree with 6+ years, Master's degree with 3+ years, or PhD with postdoctoral studies in scale-up and manufacturing of polymer materials or biomaterials. Proficiency with electrospinning equipment is preferred and experience with electrospraying, extrusion techniques, and other processes, including covalent conjugation and synthesis a plus. Strong analytical and problem-solving skills. Excellent communication skills, both written and verbal, with a keen attention to detail. Ability to work collaboratively in a fast-paced, innovative environment. Industry experience in a GMP environment is preferred. Familiarity with plant proteins and food science preferred. Benefits: Comprehensive health insurance, dental insurance, and vision insurance. Opportunities for professional growth and development. Collaborative and supportive company culture. Cutting-edge research environment with state-of-the-art equipment. Application Process: Please submit a resume and cover letter via LinkedIn. Applications will be reviewed on a rolling basis until this position is filled. If you do not send both a resume and a cover letter, your application will not be considered. Research shows that women, BIPOC, and LGBTQIA+ candidates are less likely to apply for positions if they don't meet the exact criteria that have been specified in writing. Your skills matter - they matter to us and we believe that our diversity, uniqueness, and individual experiences and perspectives make us an impactful organization. We look forward to hearing from you!

This position is responsible for formulating liquid and lyophilized dosage forms for protein therapeutics to support preclinical and clinical needs. The candidate must be proficient in analytical techniques used for protein characterization and stability testing. The candidate performs developmental studies for protein therapeutics, prepares data summaries and writes technical reports documenting various aspects of protein formulation development. Education and Qualifications BS or MS in biochemistry, biophysical chemistry, pharmaceutical science, physical chemistry, chemical engineering or a related field with 1-3 years of analytical development and/or protein formulation experience in biotech or pharmaceutical industry is required. Prior experience in development of protein formulations and stability assessment is preferred. Candidates should have hands-on experience in analytical techniques used for protein characterization and stability testing (HPLC, capillary electrophoresis, IcIEF, DSC, DLS, HIAC, MFI). The candidate should also have strong communication, documentation and report writing skills. Top Skills Required Formulation development of protein therapeutics Proficient analytical techniques used for protein characterization strong communication, documentation and report writing skills Knowledge of: HPLC, CE-SDS, IcIEF, DSC, DLS, HIAC, and MFI. Job ID - 25-36719 About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Innova Solutions has a client that is immediately hiring for a Scientist Fulltime - Contract Duration: 12 Months As a Scientist, you will: Job Description: Preferred Qualifications: PhD in pharmacology, biochemistry, molecular biology, or a related discipline. Expertise in enzymology, ligand binding kinetics, and mechanism-of-action studies. A deep and broad understanding of the development, validation & execution of a wide array of binding & functional activity-based assays such as TR-FRET, FP, PCR etc. Experience in evaluation and implementing new technologies to enhance screen capabilities and assay performance for small molecules and/or oligonucleotides. Proficiency in assay development to screen and characterize covalent inhibitors is a plus. Experience with microplate readers such as PerkinElmer Envision and automated liquid handling systems including Multidrop, acoustic dispensers, and digital dispensers. Expertise in handling, analyzing and visualizing assay data sets and proficient in software platforms such as GraphPad Prism. Drug discovery research experience in diverse target classes is a plus but not required. Top 3 Must Have Skill Sets: Experience in evaluation and implementing new technologies to enhance screen capabilities and assay performance for small molecules. A deep and broad understanding of the development, validation & execution of a wide array of binding & functional activity-based assays such as TR-FRET, FP, PCR etc. Day to Day Responsibilities: Contribute to the assay strategies and apply a variety of scientific principles and concepts to the assay design, assay development, and troubleshooting in support of small molecule drug discovery. Develop and execute biochemical assays and convert into high-throughput screening (HTS) format to enable HTS campaign and meet project goals. Apply sophisticated biochemical and biophysical assay techniques to develop and perform potency, kinetic, and mechanistic assays for hits validation, compound-target engagement, and SAR study. Advance biochemical/biophysical assay screening capabilities and evaluate new assay technologies and experimental approaches using scientific theory and technical literature. Thank you! Harish Yadav Phone: ************ ******************************** PAY RANGE AND BENEFITS: Pay Range*: $40.00-$44.00 per hour. *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: Named One of America's Best Employers for New Grads by Forbes (2024 Named One of the Best Companies to Work For by U.S. News & World Report (Private Companies List, 2024-2025) One of the Largest IT Staffing Firms in the US - Ranked #3 by Staffing Industry Analysts (SIA, 2024) One of the Largest Staffing Firms in the US - Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, & HireGenics) Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023) One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024) AWS Advanced Tier Services Partner with 100+ certifications Website: ******************************** Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at ********************** or **************. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

LinkedIn is the world's largest professional network, built to help members of all backgrounds and experiences achieve more in their careers. Our vision is to create economic opportunity for every member of the global workforce. Every day, our members use our products to make connections, discover opportunities, build skills, and gain insights. We believe amazing things happen when we work together in an environment where everyone feels a true sense of belonging and that what matters most in a candidate is having the skills needed to succeed. It inspires us to invest in our talent and support career growth. Join us to challenge yourself with work that matters at the cutting edge of AI. At LinkedIn, our approach to flexible work is centered on trust and optimized for culture, connection, clarity, and the evolving needs of our business. The work location of this role is hybrid, meaning it will be performed both from home and from a LinkedIn office on select days, as determined by the business needs of the team. Job Description: As a Staff AI Scientist, you will play a pivotal role in advancing LinkedIn's efforts in cutting-edge AI research and development, focusing on large-scale foundation models and AI innovations. You will specialize in developing, training, and optimizing foundation models, including Large Language Models (LLMs), utilizing state-of-the-art deep learning architectures such as multi-billion parameter transformers and scaling them to serve LinkedIn's global user base. Your work will involve the design and deployment of high-performance AI systems, leveraging GPUs and other hardware accelerators for large-scale training and inference. You will collaborate with a world-class team of researchers and engineers to develop and advance the next generation of AI models to push the boundaries of AI at scale, working on complex problems such as distributed training, model parallelism, and system co-design. A successful candidate will be comfortable operating at the intersection of AI research and engineering, with a deep understanding of the latest advancements including but not limited to large model training, post-training techniques for planning and reasoning, fine-tuning strategies, reinforcement learning techniques. Responsibilities: • Lead and contribute to the research, design, and development of large-scale foundation AI models, focusing on LLMs, transformer architectures, and cutting-edge AI systems. • Publish the findings and innovations as the latest academic and industry research in top notch core AI venues such as ICML, NeurIPS, ICLR, ACL,, patents, and conferences as appropriate. • Stay abreast of the latest academic and industry research, applying relevant findings to improve LinkedIn's AI capabilities. • Innovate in large-scale model training, leveraging GPUs and specialized hardware for optimal performance. • Develop and maintain scalable AI pipelines, optimizing training and inference workflows to handle vast amounts of data. • Mentor junior engineers and contribute to team growth and knowledge sharing. • Collaborate with cross-functional teams of machine learning engineers, infrastructure engineers, and AI researchers to deliver impactful AI innovations across LinkedIn's products. Basic Qualifications: • Bachelor's degree in Computer Science or related technical field or equivalent practical experience • 4+ years of experience with programming languages such as Java, Python, etc. • 4+ years of experience in machine learning or AI engineering. • 4+ years of experience in the design and development of algorithmic solutions. Preferred Qualifications: • 6+ years of hands-on experience in large-scale model training, model-system co-design, or large AI systems. • PhD in Computer Science, Machine Learning, or a related technical discipline with a focus on advanced AI/ML techniques • Proven experience in building and optimizing large-scale AI/ML models using frameworks such as PyTorch, PySpark, and CUDA. • Proven track record of publications in top notch core AI venues including but not limited to ICML, NeurIPS, ICLR, ACL. • Expertise in distributed training, model parallelism, and hardware acceleration for AI workloads, including GPUs and TPUs. • Demonstrated ability to solve complex AI challenges in large-scale environments, optimizing models for efficiency and scalability. • Strong proficiency in AI system design, model optimization, and the development of production-quality AI pipelines. • Published work in AI research or significant contributions to industry-leading AI technologies. • Excellent communication skills and a demonstrated sense of ownership over key AI projects. Suggested Skills: • Large Language Models (LLM) • Generative AI (GAI) • AI Research and Development • GPU and Hardware Acceleration • Distributed AI Systems and Model Parallelism • You Will Benefit From Our Culture: We strongly believe in the well-being of our employees and their families. That is why we offer generous health and wellness programs and time away for employees of all levels. LinkedIn is committed to fair and equitable compensation practices. The pay range for this role is $164,000 - $268,000. Actual compensation packages are based on several factors unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include an annual performance bonus, stock, benefits, and/or other applicable incentive compensation plans. For more information, visit LinkedIn Benefits. Equal Opportunity Statement We seek candidates with a wide range of perspectives and backgrounds and we are proud to be an equal opportunity employer. LinkedIn considers qualified applicants without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, marital status, pregnancy, sex, gender expression or identity, sexual orientation, citizenship, or any other legally protected class. LinkedIn is committed to offering an inclusive and accessible experience for all job seekers, including individuals with disabilities. Our goal is to foster an inclusive and accessible workplace where everyone has the opportunity to be successful. If you need a reasonable accommodation to search for a job opening, apply for a position, or participate in the interview process, connect with us at accommodations@linkedin.com and describe the specific accommodation requested for a disability-related limitation. Reasonable accommodations are modifications or adjustments to the application or hiring process that would enable you to fully participate in that process. Examples of reasonable accommodations include but are not limited to: -Documents in alternate formats or read aloud to you -Having interviews in an accessible location -Being accompanied by a service dog -Having a sign language interpreter present for the interview A request for an accommodation will be responded to within three business days. However, non-disability related requests, such as following up on an application, will not receive a response. LinkedIn will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by LinkedIn, or (c) consistent with LinkedIn's legal duty to furnish information. Pay Transparency Policy Statement As a federal contractor, LinkedIn follows the Pay Transparency and non-discrimination provisions described at this link: ******************************** Global Data Privacy Notice for Job Candidates This document provides transparency around the way in which LinkedIn handles personal data of employees and job applicants: ***************************************

Dinamo is building a new category of high-resolution DNA methylation analysis platform to decode the epigenome and bring clarity to autoimmune disease. We combine molecular biology, engineering, and advanced analytics to develop precision tools that replace ambiguity with insight. Join us to help transform how medicine understands and treats complex diseases. Role Description This role involves ML/AI methods development, data science, statistics, and data visualization. This is a full-time on-site role at our lab in San Carlos, CA. No remote, no hybrid. Minimum Requirements PhD or Masters in bioinformatics, computational biology, or related field 5+ years of experience in bioinformatics, computational biology, statistics, and/or data science Evidence (products, publications, patents, open source projects) of original computational / statistical / modeling contributions in the domains of autoimmune diseases, epigenetics, and/or transcriptomics with high-dimensional / high-noise data Evidence of cold starting projects in a commercial settings, executing extensive benchmark studies, or otherwise solving challenging / long-standing problems Fluency and aptitude in Secondary to tertiary bioinformatics analysis, data science, and machine learning with NGS data Implementation with with Python, plus at least R or one compiled language Distributed / cloud / high-performance computing or workflow managers

Tencent Games was established in 2003. We are a leading global platform for game development, operations and publishing, and the largest online game community in China. Tencent Games has developed and operated over 140 games. We provide cross-platform interactive entertainment experience for more than 800 million users in over 200 countries and regions around the world. Honor of Kings, PUBG MOBILE, and League of Legends, are some of our most popular titles around the world. Meanwhile, we actively promote the development of esports industry, work with global partners to build an open, collaborative and symbiotic industrial ecology, and create high-quality digital life experiences for players. Level Infinite is Tencent's global gaming brand. It is a global game publisher offering a comprehensive network of services for games, development teams, and studios around the world. We are dedicated to delivering engaging and original gaming experiences to a worldwide audience, whenever and wherever they choose to play while building a community that fosters inclusivity, connection, and accessibility. Level Infinite also provides a wide range of services and resources to our network of developers and partner studios around the world to help them Responsibilities: 1. Responsible for the research and development of algorithms and models for speech recognition, speech synthesis, and speech cloning in minor languages, including but not limited to the implementation and improvement of acoustic models, vocoder algorithms, and their optimization in real-world scenarios. 2. Keep up with cutting-edge technology research, integrating business planning to continuously explore innovations in speech synthesis technology and application scenarios. 3. Apply relevant algorithmic results to various scenarios such as speech, speech translation (S2TT, S2ST), and virtual humans. Requirements: 1. Over 5 years of research and work experience in speech synthesis or speech cloning, with a background in speech, signal processing, computer science, or related fields. 2. Master's or PhD in Computer Science, Computational Linguistics, Artificial Intelligence, or related fields. 3. Deep understanding of TTS and speech cloning principles, mastery of the latest speech technology, and extensive involvement in the development and implementation of cutting-edge speech synthesis or speech cloning algorithms. 4. Experience in high-expressiveness speech synthesis, style transfer, voice conversion, and emotional synthesis is preferred. 5. Proficient in deep learning, neural networks, and related open-source tools and frameworks (such as TensorFlow, PyTorch). 6. Strong logical thinking, excellent analytical and communication skills, high enthusiasm for technology, self-driven, and pursuit of excellence. 7. Strong team collaboration and communication skills, able to work closely with team members to drive project progress. 8. Passionate about the gaming industry with a certain level of understanding of the gaming field. Equal Employment Opportunity at Tencent As an equal opportunity employer, we firmly believe that diverse voices fuel our innovation and allow us to better serve our users and the community. We foster an environment where every employee of Tencent feels supported and inspired to achieve individual and common goals.

Kelly Science & Clinical is seeking a Scientist for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and medical device industries. Workplace: Onsite in Sunnyvale, CA. Position Title: Scientist, Array R&D Position Type: 6-month contract Pay rate: $35-40/ hour. Company: Kelly Science & Clinical Overview The Scientist I, Array R&D is responsible for supporting Biochip Array R&D activities, including oligonucleotide preparations and performing routine PCR. This is a central role with high visibility and involves good communication across all groups. You will establish a collaborative environment that values equity of voice, inclusive behaviors, and trusting teams. This position will be located on-site in Sunnyvale, CA. Responsibilities: Handle automated liquid handler to prepare dilutions of oligonucleotides. Perform routine PCRs, review results, and provide support with troubleshooting, problem solving,g and improving processes across multi-functional teams. Manage inventory of oligonucleotides and commonly used lab supplies and chemicals. Maintain equipment information, equipment procedures, calibration records, user logbooks, and scheduling activities. Collect, document, summarize,e and communicate data/trends on a regular basis. Assist and coordinate new equipment procurement and installation. Assist in PO invoice resolution and perform tasks related to safety and compliance initiatives in the lab as needed. Requirements Bachelor's degree in Chemistry or Biological Sciences AND 2+ years of industrial experience. Proficiency and accuracy in using pipettes and handling small volume preparations. Experience with using analytical techniques such as UV-Vis spectroscopy, fluorescence spectroscopy, pH measurements, etc. Experience with characterization of PCR and DNA microarray performance is a plus. Experience with the use of liquid handlers is a plus. Experience working in regulated environments such as GMP or CLIA is a plus Why Join Us: Competitive compensation package and potential for permanent placement following the temporary period. Opportunity to work at the forefront of biotechnology innovation in a collaborative and dynamic environment. Access to ongoing career development and networking opportunities through Kelly Science & Clinical's expansive network of industry experts and recruiters. If your qualifications align with the requirements of this role, we invite you to apply and take the next step in your career journey. Rest assured, even if this opportunity isn't the perfect match, your profile will remain within our network, ensuring you're connected to a wealth of future opportunities in the field of science and clinical research.

Job Title: Senior Research Associate - Drug Metabolism and Pharmacokinetics (DMPK) We are seeking a Senior Research Associate to join our Drug Metabolism and Pharmacokinetics (DMPK) team. This is a critical role within our core drug discovery group, providing a unique opportunity to contribute directly to the development of new drug candidates. The successful candidate will collaborate closely with a highly skilled and cross-functional team, performing in vitro metabolism assays, metabolite identification studies, and LC-MS/MS-based bioanalysis to evaluate the pharmacokinetic properties of novel chemical entities. This position offers an exciting opportunity to be part of a dynamic, innovative biopharmaceutical environment where your contributions will help advance compounds from concept to clinic. Key Responsibilities: Design and execute in vitro metabolism studies to support DMPK profiling and address key questions in drug discovery. Develop and validate analytical methods using LC-MS/MS for the separation, detection, and quantification of small molecules and peptides. Perform sample preparation and bioanalysis for both in vitro and in vivo ADME/PK studies. Conduct metabolite identification and profiling using liver subcellular fractions and other biological matrices. Present scientific findings through presentations and detailed reports to internal teams and stakeholders. Contribute to project milestones and influence early-stage drug discovery decisions. Stay current with relevant scientific literature and apply findings to internal research efforts. Maintain laboratory instruments (especially LC-MS/MS), ensuring they are operational and accessible to the team. Keep accurate and thorough experimental records in accordance with scientific and regulatory standards. Perform additional duties and contribute to cross-functional initiatives as needed. Qualifications & Experience: Bachelor's degree in Biological Sciences, Chemistry, or a related field with 5+ years of hands-on DMPK lab experience; OR Master's degree in a relevant field with 2+ years of relevant experience. Proven experience with LC-MS/MS-based sample analysis, particularly in metabolic stability, CYP inhibition, and metabolite ID studies. Hands-on experience with sample preparation and bioanalysis in support of preclinical ADME/PK studies. Strong preference for candidates with expertise in Sciex instrumentation and method troubleshooting. Demonstrated ability to independently plan, execute, and troubleshoot complex experiments. Excellent verbal and written communication skills with a collaborative and adaptable approach. Self-motivated, detail-oriented, and enthusiastic about working in a fast-paced and team-driven environment.

About Us Pace® Analytical Services Pace® makes the world a safer, healthier place. Committed to advancing the science of businesses, industries, consulting firms, government agencies, and others, Pace® offers local-level service backed by a national laboratory network. Through in-lab and emergency onsite services, Pace® ensures our air, water, soil, and more are safe. Job Description Scientist 1 Make an impact. Build a career. At Pace , everything we do is built upon an unwavering commitment to making the world a safer, healthier place. We continually work to develop innovative practices that drive sustainability and empower our partners with accurate, quality data at every critical moment and milestone. That's why we need you -- your curiosity, your talents, and your drive -- to help us advance this important work, and your career. Find your place at Pace Join us as a Scientist I, where you'll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you'll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate instruments Maintain detailed and organized documentation on all laboratory work What you'll bring Bachelor's degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience Ability to perform work in a lab or office setting, remain standing for long periods while conducting tests, work around strong smells, and wear personal protective equipment while handling samples (e.g., lab coat, safety glasses and gloves; all PPE provided by Pace ). What we promise Comprehensive benefit program, including medical, vision and dental insurance, 401(k) matching and tuition reimbursement Opportunities to build a rewarding career An inclusive culture that stands for integrity, innovation and growth Additional Information Benefits 80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance. Equal Opportunity Employer Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Pay Range/Compensation $18.00 per hour Work Schedule Monday through Friday 8 to 5.

TITLE: Research Scientist EXEMPT OR NON-EXEMPT: Exempt FULL- OR PART-TIME: Full-time PAY RANGE: $90,000 - $125,000 + bonuses REPORTS TO: Technical Director or as otherwise assigned. The Research Scientist will typically report to the Technical Director but may report to another member of Technology Management, as required. The Research Scientist is responsible for completing assigned research projects focused on the development of quantitative analytical chemistry techniques in support of Edeniq's business objectives including experimental design and conduct, data analysis, generation of meaningful conclusions and recommendations, and timely report writing. Responsibilities will also include conception and design of research projects and objectives, as well as supporting Edeniq Management in the development of technology strategy. Supervision of one or more Support Staff can be expected. Direct support of Company Intellectual Property development can also be expected. The Research Scientist will have a strong personal commitment to safety and be able to succeed in a fast-paced collaborative environment. EXPECTATIONS OF ALL EMPLOYEES: All employees of Edeniq, Inc. (“Edeniq” or the “Company”) must adhere to and follow the policies and procedures in the Company's Employee Handbook and are required to comport themselves to other Edeniq stakeholders (the Company, fellow employees, vendors, customers and other vested Company parties) with respect, support, honesty, courteousness, and hard work-"doing what we said we would do, and doing it well.” ESSENTIAL FUNCTIONS: Conducts and completes assigned research projects: Defines research objectives, milestones, and timelines. Defines project resource requirements. Writes concise research project proposals for Technical Director review and approval. Ensures project research is conducted consistent with project objectives, milestones, and timelines. Effectively manages project resources. Effectively communicates progress toward project objectives, milestones, and timelines to Technical Director and Company Management, as required. Recommends, when appropriate, revisions in project objectives, milestones, and timelines. Analyzes experimental data and generates scientifically valid conclusions and recommendations, as needed, for future research. Provides timely written reports to Company Management describing progress toward project objectives, milestones, and timelines. Provides timely final project report upon project completion. Works with Technology and Company Management to identify and pursue Intellectual Property derived from research project results. Supervises one or more members of Support Staff including direction of daily project activities, data review, coaching and counseling, and performance feedback. Remains current on relevant scientific literature and intellectual property landscape. Develops and maintains competitive intelligence in relevant areas. Directly supports Technology and Company Management in defining new research projects and potential new areas for development. Maintains accurate lab and data records in accordance with Company policies. Ensures a hygienic work environment, participating in lab cleanliness, organization, and other tasks. Supports and adheres to all company policies on safety, chemical hygiene, and the environment. KNOWLEDGE, SKILLS AND ABILITIES: Demonstrated ability to develop and validate novel and robust quantitative analytical chemistry methods. Extensive knowledge of modern analytical techniques: Chromatography (including hyphenated techniques) Spectroscopy Near Infrared (NIR) and Infrared (IR) Raman Ultraviolet and visible (UV/Vis) Fluorescence Nuclear Magnetic Resonance (NMR) Exceptional quantitative data analysis and computer skills: Statistics, including working knowledge of software such as MatLab Multivariate Data Analysis techniques such as Partial Least Squares (PLS) and Design of Experiment (DOE) Data reduction techniques such as Principal Components Analysis (PCA) Exposure to Machine Learning and Visualization would serve as an added recommendation Knowledge of fermentation and carbohydrate chemistry would serve as an added recommendation. Excellent verbal and written communication skills. Team player with the ability and willingness to work effectively in a fast paced, collaborative environment. Strong personal commitment to workplace safety and the environment. Requirements REQUIREMENTS: PhD in Chemistry or a closely related field. Minimum three (3) years' experience in a post-graduate research environment. Must possess and maintain a valid driver's license. PHYSICAL REQUIREMENTS - LAB: Must be able to perform the essential functions with or without accommodations. This position is considered light work, exerting up to 5-10 pounds of force or lifting frequently in a laboratory (and up to 30-40 pounds of lifting infrequently), and work is primarily done upright at a chest high lab counter for lengthy periods of time working with chemicals, beakers, flasks, and other lab equipment: Physical Task Extending hands and arms in any direction - Frequently, up to 75% of the time Move, Traverse - Frequently move about the lab Remain upright at lab counter - Frequently, up to 50% of the time Apply pressure to an object with the fingers and palm - Frequently, up to 50% of the time Raising objects from a lower to a higher position or moving objects horizontally from position to position - Frequently, up to 20% of the time Must be able to handle various chemicals safely and follow safety policies and procedures May handle hazardous and non-hazardous chemicals; exposed to liquids, fumes, dust, and gasses We are an Equal Opportunity Employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. Salary Description $90,000 - $125,000

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to: * Career development with an international company where you can grow the career you dream of. * Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. * An excellent retirement savings plan with high employer contribution · Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. * A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. * A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it's glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. The Opportunity This position works out of our Santa Clara or Sylmar, CA locations with our Global Data Science & Analytics team with the Abbott Medical Device business. You will be responsible for working on complex problems in the field of life-saving implantable medical devices. You will work with different types of data, developing creative ways to analyze and present your results. You will use machine learning, artificial intelligence, statistical modeling, data mining, and visualization techniques to provide analytics solutions to a wide range of challenging projects. As a key member of the team, you will develop solutions to curate and analyze large quantities of medical data. You will work on projects that quantify real-world clinical and economic outcomes of life-saving therapies used in chronic disease states. You will collaborate effectively with internal stakeholders and cross-functional teams. You will present solutions and insights in concise and effective manner to technical and non-technical audiences. You will work on a diverse team with scientists, analysts, engineers, and physicians on a variety of projects and act as a subject matter expert for data science. You will support preparation of scientific conference presentations and publications. Main responsibilities will include: Data Analytics * Curating and analyzing complex healthcare data (such as insurance claims, electronic health records, imaging data, medical device data, etc) * Designing and executing data analyses for real-world evidence generation * Performing integrative analyses of clinical and device data from large patient cohorts * Translating real-world observations into clinical actionable insights using precision medicine, phenotyping, machine learning, and artificial intelligence * Applying scientific knowledge on data modeling, data analytics, predictive algorithms, and other data science principles * Researching and developing AI/ML and Deep Learning algorithms * Solving analytical problems and effectively communicating methodologies and results * Creating dashboards and visualizations of processed data to identify trends Strategy and Communication * Translating project needs and goals into a data-driven analytical approach * Understanding the context of big data and its implications around privacy * Working autonomously in a fast-paced environment * Collaborating with a broad range of technologists and support personnel both within and outside of Abbott * Supporting digital health and data science initiatives * Preparing protocols and reports, conference presentations, and scientific manuscripts * Communicating with regulatory and reimbursement agencies on study design and results * Presenting complex concepts to internal stakeholders with varied backgrounds Required Qualifications * Associates Degree (± 13 years) * Minimum 7 years of experience Preferred Qualifications * Ph.D. and 2+ years of experience or MS and 5+ years of experience in biomedical engineering, health sciences, bioinformatics , data science, computer science or related field * Strong data wrangling and analysis skills * Strong knowledge of statistical methods * Experience with analytical software tools such as R, SAS, Python, SQL. Familiarity with cloud platforms such as Databricks is a plus * Experience with big-data architecture, operating systems and tools for big-data analytics * Hands-on knowledge of contemporary machine learning, pattern recognition and data-mining techniques. * Ability to come up with innovative data analysis and presentation strategies * Strong oral and written communication skills * Experience working in healthcare/medicine * Experience working in a regulated environment a plus The base pay for this position is $86,700.00 - $173,300.00. In specific locations, the pay range may vary from the range posted.

Full-time Description Lyons Magnus leads the food industry with creativity and innovation, crafting top-quality products across all manufacturing phases, from raw materials to marketing. With over 2,000 diverse items for industrial ingredient and food service sectors, Lyons caters to leading restaurant chains nationally and internationally. At Lyons, our diverse and talented staff is the heart of our organization. We foster a thriving work environment where employees are engaged in shaping both the company's and their own future. This position is responsible for product development and commercialization of new products, product renovation and product maintenance projects. The R&D Scientist is responsible to manage project deliverables to contribute to achieving short and long term departmental and company objectives. This position will work closely with cross-functional partners in Marketing, Consumer Insights and Sales to carry out product design and development work leading to products that deliver on consumer and customer needs. The position works collaboratively with manufacturing, Quality and Supply chain functions to assure products consistently deliver on product design. Salary Range: $100,000 - $115,000/ per year Shift: Day Schedule: Monday - Friday Core Responsibilities: Direct the technical commercialization of new Lyons Magnus and customer products. Direct the coordinated development of new products and improvements of current products to deliver on objectives of the annual business plans. Apply sound culinary and scientific techniques to design products with consumer/customer-valued attributes. Lead and manage multiple development projects using detailed investigations, well-thought-out experimental design, sound scientific techniques and data-based decision making. Investigate for product and process challenges; provide creative solutions to solve challenges in development and commercialization. Establish professional relationships with fellow scientists and team members of our customers and suppliers. Work with other departments (Manufacturing, Engineering, Maintenance, Quality and Purchasing) to determine equipment, materials and processes necessary to produce products to maximize capacity and optimize product quality and differentiation. Assure technically sound sensory panels are conducted for product development, shelf-life studies, improving/maintaining present products and competitive testing. Identify and complete technical study of ingredients, suppliers, co-packers relevant to meeting project objectives and meeting Lyons Magnus standards. Develop supportive relationships with cross-functional peers within the Lyons Magnus marketing, sales, manufacturing, sourcing, engineering, finance, and business support functions. Build partnerships and leverage technical expertise of ingredient suppliers. Travel to manufacturing sites when deemed necessary to oversee plant trials and/or scale-up of critical products. Provide product demonstrations and presentations to customers when requested. Project management, alignment within all cross-functional departments for product commercialization. Gather, communicate and monitor sales forecasts for limited time offers and new product introductions. Update internal departments with project details, timelines, and customer requirements. Customer interface with select accounts. Requirements Knowledge, Skills and Abilities Strong interpersonal skills and demonstrated ability to work with cross functional teams, internally and externally (e.g. research institutes, representatives of processing and produce industries, suppliers, laboratories, etc.). Ability to work independently and as part of a technical team. Individual must have strong product development skills in ingredient functionality, material selection, and formulation. Candidate must expertly plan and conduct trials, data collection, and interpret results to drive program and technical knowledge forward, developing robust action plans, risk assessments, and contingency planning. Demonstrated problem-solving skills (pays attention to details and effort to understand causes instead of just the effects) and creativity for developing innovative solutions and applications. Excellent written and oral communication skills with strong emphasis on technical presentations and reports. Excellent communication to external partners including customers and vendor network. Ability to effectively manage multiple projects under short timelines to produce commercially viable solutions. Proven ability to multi-task in a fast-paced environment. Strong project management skills, influential savvy, and perseverance. Consistently meet deadlines. Self-motivated, self-starter Ability and willingness to work extended or odd hours when necessary. Ability to thrive in a fast paced, dynamic working environment. Mature, friendly, enthusiastic, and motivated team member. Effective written and oral communication skills. Excellent work ethic with proven ability to effectively balance multiple priorities. Ability to establish credibility with others. Ability to recognize and support the organizations preferences and priorities. Proficient in Excel, Access, Power Point, and ERP systems. Analytics skills, developing and building data models. Strong passion for science and creative problem solving. Technical knowledge with good reasoning and sound judgment abilities. Education and/or Experience Bachelor's degree required, advanced degree preferred, in Food Science, Dairy Science or an equivalent science program. Minimum 5 years' experience in an industrial or applied research environment in the area of food science and technology, processing, or new product development. Experience with Food Service and QSR is desired. Prior experience with customer interaction is required. Additional InformationOur compensation program is designed to attract, motivate, and retain the very best people. Lyons Magnus offers a comprehensive benefits plan that include: Health, Dental Insurance, Life Insurance, Long Term Disability, Sec. 125, 401(k) plan, and more. If you meet these requirements and are eager to join a dynamic company poised for further growth, please respond with your cover letter, and salary requirements. To learn more about Lyons Magnus, LLC its products and core values, visit ******************* or follow us on Instagram or LinkedIn Lyons Magnus is an Equal Opportunity Employer and with opportunities for advancement. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories. *This organization participates in E-Verify. Salary Description $100,000 - $115,000/year

At Saputo, we bring good to the table by making high-quality products, investing in our people, and supporting communities around the world . As a top 10 global dairy processor, we value contributions that matter and strive to foster an inclusive, growth-driven work environment. Ready to bring your best? The Research Scientist role will lead, under the guidance and coaching of their manager, the successful development and execution of new and innovative cheese and dairy products. How You Will Make Contributions That Matter… Ensure the constant improvement of quality (performance) of existing products, production systems and raw materials. Provide technical product-process support to plant technologists. Coordinate the definitions of formulations for new products. Partner with cross functional partners (Marketing, Sales, Operations, Supply Chain, etc.) to ensure an efficient and successful product initiation, progression and execution. Lead complex new product development and support current product improvement. Plan and monitor plant trials, and trains others to conduct plant trials. Source and maintain vendor relationships to secure the necessary ingredients that align with Company standards. Successful commercialization of new products. Coach and review work with lower-level professionals. Problems faced are difficult and often complex. Influence others regarding product development practices and procedures. Ensure coordination and supervise the execution in the plant of new process technologies tests and new manufacturing capabilities potentially impacting the quality of products. Collaborate with technical bodies in the design of new manufacturing equipment or modifications of existing ones. Perform other work assigned. You are best suited for the role if you have the following experience, skills, and qualifications... Bachelor's degree (or Master's degree) in Food Science plus 3-5 years related experience (R&D or production in the cheese (preferred) or dairy manufacturing industry). Experience in R&D, innovation, product, raw materials, process, technology development roles and/or as production supervisor or manager positions in the cheese or dairy manufacturing industry is required. Successful track record and proven experience in product/process development from plant trials to successful execution to market (is a plus). Result-oriented with strong passion for creativity and innovation within a complex driven environment. Dynamic, flexible, proactive approach and ability to work effectively in high - pressure situations within strict deadlines. Strives for high standards, seeks innovative solutions, drives continuous improvement of ingredients, semi-finished and finish products, processes and demonstrates a high degree of attention to detail. Strong interpersonal skills with ability to influence with integrity through persuasive communication to win support at senior levels within R&D and across various functional areas, such as production manufacturing & QA departments. Strong people and project management skills to effectively and efficiently drive a complex program. Excellent Excel and PowerPoint experience. Familiarity with SAP Architecture/planning system is a plus. Proficient in use of information. Microsoft Excel, BI and advanced analytical tools such as PowerBI. Travel up to 50% (across California & Las Cruces, NM) We Support and Care for Our Employees by Providing Them With… Development opportunities that enhance their career fulfillment through employee recognition and incentive programs. Meaningful compensation & benefits that help them care for their families that include medical, dental and vision insurance, Employee Assistance Program (EAP), 401K, employee share ownership plan, and paid time off. Opportunities to contribute to your community via a Volunteer Time Off (VTO) Program, site engagement activities and enhance the lives of others through Saputo products Work on a smoke-free campus that promotes a healthy and wellness focused lifestyle. Salary Range: $85,370-$112,050. Salary offers vary commensurate with experience, skills, education, and training In the USA, Saputo ranks among the top three cheese producers and is one of the top producers of extended shelf-life and cultured dairy products, with a portfolio of well-loved brands such as Stella, Frigo Cheese, Montchevre, Stella, and Treasure Cave. We also boast a strong foodservice presence, partnering with reputable chain restaurants and broadline distributors. Whether your expertise lies in manufacturing, operations, supply chain, sales, quality assurance, or in any other function, your role is integral to our success. You will make contributions that matter, all while working alongside colleagues who genuinely care about your success and who will roll up their sleeves to help. Saputo Cheese USA Inc. and Saputo Dairy Foods USA, LLC endeavors to make CareersUSA.Saputo.com accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact Human Resources at ************ or email *******************************. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. Saputo Cheese USA Inc. and Saputo Dairy Foods USA, LLC are equal opportunity employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you'd like more information on your EEO rights under law, please visit ************* To review the Saputo Cheese USA Inc. and Saputo Dairy Foods USA LLC Privacy Notice for California applicants, please visit our Corporate website associated section by clicking here (English) or here (Spanish).

At Saputo, we bring good to the table by making high-quality products, investing in our people, and supporting communities around the world . As a top 10 global dairy processor, we value contributions that matter and strive to foster an inclusive, growth-driven work environment. Ready to bring your best? The Research Scientist role will lead, under the guidance and coaching of their manager, the successful development and execution of new and innovative cheese and dairy products. How You Will Make Contributions That Matter… Ensure the constant improvement of quality (performance) of existing products, production systems and raw materials. Provide technical product-process support to plant technologists. Coordinate the definitions of formulations for new products. Partner with cross functional partners (Marketing, Sales, Operations, Supply Chain, etc.) to ensure an efficient and successful product initiation, progression and execution. Lead complex new product development and support current product improvement. Plan and monitor plant trials, and trains others to conduct plant trials. Source and maintain vendor relationships to secure the necessary ingredients that align with Company standards. Successful commercialization of new products. Coach and review work with lower-level professionals. Problems faced are difficult and often complex. Influence others regarding product development practices and procedures. Ensure coordination and supervise the execution in the plant of new process technologies tests and new manufacturing capabilities potentially impacting the quality of products. Collaborate with technical bodies in the design of new manufacturing equipment or modifications of existing ones. Perform other work assigned. You are best suited for the role if you have the following experience, skills, and qualifications... Bachelor's degree (or Master's degree) in Food Science plus 3-5 years related experience (R&D or production in the cheese (preferred) or dairy manufacturing industry). Experience in R&D, innovation, product, raw materials, process, technology development roles and/or as production supervisor or manager positions in the cheese or dairy manufacturing industry is required. Successful track record and proven experience in product/process development from plant trials to successful execution to market (is a plus). Result-oriented with strong passion for creativity and innovation within a complex driven environment. Dynamic, flexible, proactive approach and ability to work effectively in high - pressure situations within strict deadlines. Strives for high standards, seeks innovative solutions, drives continuous improvement of ingredients, semi-finished and finish products, processes and demonstrates a high degree of attention to detail. Strong interpersonal skills with ability to influence with integrity through persuasive communication to win support at senior levels within R&D and across various functional areas, such as production manufacturing & QA departments. Strong people and project management skills to effectively and efficiently drive a complex program. Excellent Excel and PowerPoint experience. Familiarity with SAP Architecture/planning system is a plus. Proficient in use of information. Microsoft Excel, BI and advanced analytical tools such as PowerBI. Travel up to 50% (across California & Las Cruces, NM) We Support and Care for Our Employees by Providing Them With… Development opportunities that enhance their career fulfillment through employee recognition and incentive programs. Meaningful compensation & benefits that help them care for their families that include medical, dental and vision insurance, Employee Assistance Program (EAP), 401K, employee share ownership plan, and paid time off. Opportunities to contribute to your community via a Volunteer Time Off (VTO) Program, site engagement activities and enhance the lives of others through Saputo products Work on a smoke-free campus that promotes a healthy and wellness focused lifestyle. Salary Range: $85,370-$112,050. Salary offers vary commensurate with experience, skills, education, and training In the USA, Saputo ranks among the top three cheese producers and is one of the top producers of extended shelf-life and cultured dairy products, with a portfolio of well-loved brands such as Stella, Frigo Cheese, Montchevre, Stella, and Treasure Cave. We also boast a strong foodservice presence, partnering with reputable chain restaurants and broadline distributors. Whether your expertise lies in manufacturing, operations, supply chain, sales, quality assurance, or in any other function, your role is integral to our success. You will make contributions that matter, all while working alongside colleagues who genuinely care about your success and who will roll up their sleeves to help. Saputo Cheese USA Inc. and Saputo Dairy Foods USA, LLC endeavors to make CareersUSA.Saputo.com accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact Human Resources at ************ or email *******************************. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. Saputo Cheese USA Inc. and Saputo Dairy Foods USA, LLC are equal opportunity employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you'd like more information on your EEO rights under law, please visit ************* To review the Saputo Cheese USA Inc. and Saputo Dairy Foods USA LLC Privacy Notice for California applicants, please visit our Corporate website associated section by clicking here (English) or here (Spanish).

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA writing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, please apply via LinkedIn. Job Description: Senior Research Assistant / Associate Scientist, Assay Development / Analytical Development Position Overview: The SRA/Associate Scientist in Assay Development and Analytical Development will play a critical role in the development, qualification, and validation of analytical methods to support our RNA editing programs. The successful candidate will work under the guidance of an assay development scientist to develop custom assays for the analysis of samples, including AAVs, cells, and tissues, and will ensure that all methods and processes are in accordance with FDA and ICH guidelines. This role also involves aiding in method transfer and oversight of sample analysis at Contract Research Organizations (CROs), as well as drafting Standard Operating Procedures (SOPs), method development reports, and regulatory documents. Key Responsibilities: Method Development, Qualification, and Validation: Support the development, qualification, and validation of analytical methods in accordance with FDA and ICH guidelines. Ensure robust and reproducible methods for the analysis of AAVs, cells, and tissues. Develop, optimize, and implement analytical methods for the characterization, release, and stability testing of Amber's gene therapy. Sample Analysis: Support drug absorption, distribution, metabolism, and excretion studies. Perform analysis of AAVs, cells, and tissues to support various stages of research and development. Interpret and present analytical data to support decision-making processes. Lead efforts to streamline and optimize sample storage and processing, as well as establishing and maintaining critical reagent stocks and cell banks. Method Transfer and Oversight: Ensure the accuracy and consistency of sample analysis conducted by external partners. Provide technical guidance and support to CROs as needed. Documentation and Reporting: Draft and review SOPs, method development reports, and regulatory documents. Maintain accurate and detailed records of all experiments and analyses. Qualifications: B.A./B.S. or M.S. in Molecular Biology, Biochemistry, Analytical Chemistry, or a related field. 5+ years of experience in assay development and analytical development in the biotechnology or pharmaceutical industry. Experience using automated systems to perform high-throughput RNA extractions. Experience with RNA-based therapies is highly desirable. Familiarization with FDA and ICH guidelines for method development, qualification, and validation. Hands-on experience with analytical techniques such as PCR, qPCR, dd PCR, ELISA, and cell-based assays and detection methods such as fluorescence, luminescence, and ECL. Prior history in compiling and analyzing data and generating reports that are routinely presented to project teams and executive management to enable decision-making. Experience writing transfer test methods and regulatory filings is a plus. Ability to work effectively in a collaborative, fast-paced environment. Preference will be given to those who display: High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. Team-oriented thinking. Demonstrated excellence in small team environments, including a “no task is too small” attitude. If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.