Genesis Molecular AI is assembling a world-class computational chemistry team to revolutionize drug discovery through cutting-edge machine learning and biophysical simulation. We are seeking a Senior CADD Scientist to join our team, working directly with scientists in our state-of-the-art wet lab and with our distributed computational chemistry and CADD science teams across the US. What You Will Do (Key Responsibilities) - Utilize a combination of industry-standard and proprietary AI-powered CADD tools to guide small molecule drug discovery programs across a diverse target portfolio, including novel targets with limited chemical precedents. - Use approaches like virtual screening, molecular simulation, and potency and ADMET prediction to support key decision-making in drug discovery efforts. - Collaborate closely with medicinal chemists in molecular design and the development of project-specific computational approaches. - Act as a cross-team connector, effectively communicating between our computational chemistry and medicinal chemistry teams to ensure seamless information flow and collaborative decision making. - Adapt to a fast-paced environment where innovation and quick iteration are encouraged. What you’ll bring - PhD in Computational Chemistry, Structural Biology, or a related field. This particular role may also be suitable for PhD-level scientists with degrees in organic or medicinal chemistry with extensive experience in the lab, who have transitioned into industry roles in CADD. - Deep understanding of structure-based drug design and protein-ligand interactions. - Proficiency with industry-standard CADD tools such as MOE, PyMOL, and Schrodinger Suite. - Minimum of 2+ years of industry experience as a CADD scientist in pharma or biotech, with hands-on experience in active drug discovery programs. - Onsite in our San Diego lab is preferred for this role, to be able to collaborate with our scientists. We are open to remote team members too. What we offer - Competitive Pay - Health Care Plans (including Medical, Dental, and Vision, fully covered for the employees) - Stock Option Eligibility - 401(k) Plan - Open PTO Policy - Paid Company Holidays - Subsidized lunch and snacks at our offices About Genesis Molecular AI Genesis Molecular AI is pioneering foundation models for molecular AI to unlock a new era of drug design and development. The company’s generative and predictive AI platform, GEMS (Genesis Exploration of Molecular Space), integrates AI and physics into industry-leading models to generate and optimize drug molecules, including the breakthrough generative diffusion model Pearl for structure prediction. Genesis has raised over $300 million from leading AI, tech and life science-focused investors, signed multiple AI-focused research collaborations with major pharma partners, and is deploying GEMS to advance an internal therapeutics pipeline for a variety of high-impact targets. Genesis is headquartered in San Mateo, CA, with a fully integrated laboratory in San Diego. We are proud to be an inclusive workplace and an Equal Opportunity Employer.

At WISEcode, we're a well-funded, dynamic startup. WISEcode makes personalized nutrition a reality based on the facts – what truly is in our food — and marries this data with your preferences. Powered by AI and the world’s best food and nutrition database, WISEcode embraces the fact that we are all different, have different dietary needs, objectives, and preferences, and should not be at the mercy of market spin or “expert” opinion. Every one of us should have the information we need to make the best decisions for ourselves. About the Role WISEcode is a food tech AI company building the world’s most comprehensive food data platform. We map 15,000 data points per product to power a scientific logic engine that determines how food is understood. At the center of this system is the Code Library—a growing set of computational models that translate ingredients and nutrients into structured intelligence. As an Applied Computational Nutrition Scientist, you are a model builder. You will use our proprietary Code Builder to explore structures, refine assumptions, and shape the behavior of the system that serves as the "Bloomberg for Food." The Applied Computational Nutrition Scientist role represents a fundamental shift in food science: moving away from linear hand-offs between scientists and engineers toward an interactive, rapid modeling loop. The role reports directly to the VP of Science. What You’ll Do - Scientific Modeling: Design, build, and iterate nutrition codes within our AI-based platform. You will manage the full " interactive modeling loop" : Hypothesis →Build→ Evaluate→ Refine. - Logic Architecture: Transition raw food data into structured, interpretable intelligence by exploring model structures, identifying edge cases, and refining scoring assumptions. - Library Governance: Own the integrity of the Code Library as a strategic asset. Ensure every model is architected for cross-product consistency and serves as the "ground truth" for our AI systems. - Iterative Experimentation: Test model variations and interpret AI-generated structures to improve accuracy and real-world relevance. - Partner Ecosystems: Lead collaborative code-building sessions with external partners, guiding them through the creation of shared modeling frameworks. - Product Translation: Partner with the Product team to ensure that the scientific logic of our "Intelligence Layer" is documented for simplified, high-impact consumer narratives. What We’re Looking For Requirements - Domain Expertise: BS or MS in Nutrition, Food Science, or a related field with deep ingredient and food processing knowledge. - Technical Experience: 2–3 years of experience in a technical, analytical, or data-driven role. - Computational Modeling: Strong comfort with math, structured logic, and quantitative decision rules (thresholds, scoring systems, rule-based logic). - Platform Fluency: Ability to work within a proprietary computational system, interpreting outputs and refining system behavior. - Project Coordination: Proven experience supporting or coordinating projects: staying organized, tracking details, and delivering on time in a team setting. - Facilitation & Communication: Strong organization and facilitation skills used to support team projects and help others succeed. You are a collaborative, proactive, and highly reliable communicator. - Mindset: A natural explorer who enjoys identifying edge cases and refining scientific assumptions through rapid iteration. Successful Profile - Model Builder: You thrive on exploring structures and shaping system behavior rather than just following predefined instructions. - From Lab to Field: You take complex concepts out of the lab and into the field, ensuring rigorous nutritional math translates into functional utility. - The Translator: You have a product-centric mindset, intuitively seeing how a scoring system impacts a B2B dashboard or consumer app. - Operational Excellence: You maintain the highest standards of data integrity while moving with the speed of an interactive modeling environment. WISEcode is an equal opportunity employer. Consistent with applicable law, all qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application process, please send a request to WISEcode Human Resources at jobs@wisecode.ai.

• Join an amazing team that is consistently recognized for our achievements and culture • Own and lead the strategy, governance, and continual improvement of automated discovery capabilities • Ensure the CMDB remains accurate, complete, and reliable • Drive cross-functional collaboration to achieve comprehensive visibility into the IT environment • Establish standards, oversight, and optimization practices that preserve the integrity and value of CMDB data

What Sterility Assurance brings to Cardinal Health Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Sterility Assurance performs specialized technical and scientific laboratory testing to ensure the compliance and safety of the company's products. This job family develops and executes precise testing procedures and reports on results in accordance to internal and external requirements. This is fully remote position within the United States. Job Summary Under the general direction of the Director, Sterility Assurance, this role provides technical expertise and manages special projects in the areas of sterilization, sterility assurance, microbiology and analytical chemistry laboratory testing, controlled manufacturing and product evaluations to ensure the sterility and regulatory compliance of products in Cardinal Health’s Medical segment. As a subject matter expert in microbiology, sterilization, cleanroom technology and relevant regulatory requirements, this role works on cross-functional teams to develop actionable insights for ensuring quality, cost savings, operational improvements and innovation especially focused on Ethylene Oxide and Radiation Sterilization processes. Responsibilities - Demonstrates advanced understanding of quality philosophies, principles, systems, methods, tools, and standards. - Develops, and implements quality programs, including tracking, analyzing, reporting and problem solving. - Responsible for project management, coordination of activities, and SME technical support associated with controlled manufacturing, sterilization process R&D, development, optimization, and validation, as assigned. - Perform sterilization process development, chamber qualification/validation, equivalency, parametric release statistical evaluations/process maintenance and implementation activities across internal and external contract sterilizers according to ANSI/AAMI/ISO requirements. - Perform Advanced Technical Writing including authoring of study protocols/final reports and data analysis/ verification. - Responsible for project management, SME support, and coordination of activities associated with special projects (complaint investigation, regulatory compliance, cost savings, manufacturing operations, transformation/changes, etc.), and cross functional teams as assigned. - Responsible for the supplier management of contract sterilizers and support laboratories. - Responsible for advanced sterilization related nonconformance, deviation, and CAPA investigations. Perform SME technical evaluations of abnormalities in sterilization processing and batch records for product release and lead special studies in support of product release. - Authoring and maintenance of procedure, policy, and form updates within quality system. Evaluation of procedures for compliance and alignment to industry standards, performance of gap assessments, and driving of mitigation solutions and best practices. - Support and management of Sterility Assurance programs such as Environmental Monitoring, Bioburden Monitoring, Product Adoption, and Sterilization Metrics, as assigned. - Provides Sterility Assurance SME support to medical device manufacturing sites, sterilization sites, laboratories, procurement, cross functional departments and project teams. - Support and perform supplier audits including contract sterilizers, manufacturers, and microbiological and analytical laboratories. - Support regulatory compliance audits as SME. - Demonstrates understanding of the audit process including types of audits, planning, preparation, execution, reporting results and follow-up. - Plans, controls, and assures product and process quality in accordance with quality principles, which include planning processes, design control, material control, acceptance sampling and measurement systems. - Demonstrates knowledge of reliability, maintainability, and risk management, including key terms and definitions, modeling, systems design, assessment tools and reporting. - Applies problem solving and quality improvement tools and techniques, including preventive and corrective actions and how to overcome barriers to quality improvements. - Acquires and analyzes data using appropriate standard quantitative methods to facilitate process analysis and improvements. - Trains, mentors, and develops less experienced colleagues within Sterility Assurance. Qualifications - Bachelor’s degree in microbiology, biology, chemistry, biochemistry, physics, or engineering preferred, or other related scientific field or equivalent work experience preferred. - 4+ years professional experience within an FDA regulated industry, medical devices preferred. - 4+ years working experience in a quality or regulatory role preferred. - 4+ years working experience in a sterilization or sterility assurance engineering related role preferred. - Microbiology lab or clinical background experience is preferred. - Proficiency in MS Office applications and with strong project management and communication skills including scientific technical writing, preferred. - ISO 11135 (Ethylene Oxide) and ISO 11137 and 13004 (Radiation) experience preferred. What is expected of you and others at this level - Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects. - May contribute to the development of policies and procedures. - Works on complex projects of large scope. - Develops technical solutions to a wide range of difficult problems. - Solutions are innovative and consistent with organization objectives. - Completes work independently receives general guidance on new projects. - Work reviewed for purpose of meeting objectives. - May act as a mentor to less experienced colleagues. Anticipated salary range: $80,900 - $127,050 Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. - Medical, dental and vision coverage - Paid time off plan - Health savings account (HSA) - 401k savings plan - Access to wages before pay day with myFlexPay - Flexible spending accounts (FSAs) - Short- and long-term disability coverage - Work-Life resources - Paid parental leave - Healthy lifestyle programs Application window anticipated to close: 04/03/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here