Associate Director, Clinical Pharmacology City TherapeuticsAssociate Director, Clinical PharmacologyCambridge, Massachusetts$174,000–$196,000 / yearThe successful candidate will work in a highly cross-functional environment, partnering closely with Clinical Development, Regulatory Affairs, Clinical Operations, Biostatistics, Data Science, CMC and external collaborators to drive data-driven decision making and advance clinical development. Lead and execute model-informed drug development (MIDD) activities, including population PK, exposure-response, PBPK, and mechanistic PK/PD modeling, either independently or in collaboration with quantitative scientists, to support regulatory interactions and development planning.
Staff Regulatory Affairs Associate (Digital Health & AI Technologies) WhoopStaff Regulatory Affairs Associate (Digital Health & AI Technologies)Boston, MassachusettsAt WHOOP, we view total compensation as the combination of base salary, equity, and benefits, with equity serving as a key differentiator that aligns our employees with the long-term success of the company and allows every member of our corporate team to own part of WHOOP and share in the company’s long-term growth and success. Partner with Product, Engineering, and AI/ML teams to evaluate regulatory implications of new features, algorithms, health insights, claims, intended uses, and user experiences, and recommend appropriate regulatory and claims strategies.
Associate Scientific Director, Synthetic Molecule DS Project Lead 3316 Takeda Development Center AmericasAssociate Scientific Director, Synthetic Molecule DS Project LeadCambridge, MassachusettsDigital fluency and independent, responsible use of approved generative AI tools: Demonstrated ability to leverage digital tools to improve cross-functional execution, transparency, and decision readiness; uses approved generative AI tools to accelerate preparation of governance-ready materials independently and responsibly, ensuring human review, traceability, and protection of confidential information, and may coach peers on effective use within applicable policies. In Pharmaceutical Sciences, Synthetic Molecule Process Development (SMPD) we develop and leverage the scientific expertise of our diverse talent to ensure patient safety and access to medicines through the design, development, and understanding of robust, sustainable, low-cost manufacturing processes, while ensuring on-time delivery of high-quality synthetic molecule drug substance.
Associate Director, Global Regulatory Affairs - GI & Inflammation 3316 Takeda Development Center AmericasAssociate Director, Global Regulatory Affairs - GI & InflammationBoston, Massachusetts$154,400–$242,550 / yearDemonstrates strong skills with increasing independence in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies. Acceptable and independent skills in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.
Associate Director - Data Modeling 3316 Takeda Development Center AmericasAssociate Director - Data ModelingCambridge, Massachusettsdevelop knowledge graph products with functionality related to user-interfaces, views, search, LLM-augmented RAG (Retrieval Augmented Generative) conversational interfaces and other gen-AI components etc. to enable the dissemination of the knowledge & insights across R&D. As an Associate Director - Data Modeling, you will provide Data Modelling subject-matter-expertise to ensure high-quality analysis-ready data assets are created and utilized in a systematic manner for insight generation within R&D.
Associate Director, Global Labeling Lead 3316 Takeda Development Center AmericasAssociate Director, Global Labeling LeadMassachusettsThe Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU) is a key role in Global Labeling and works under the direction of the Head of Global Labeling and is: Responsible, with minimal supervision for providing regulatory expertise, strategic insight, and guidance to internal stakeholders, including Clinical, Pharmacovigilance, Legal, Scientific, Commercial, to ensure successful development and maintenance of labeling managed within PDT BU’s Global Labeling function, pertaining to pharmaceutical drug and device. In close collaboration with the Takeda R&D labeling function, oversees the direction, management and implementation of the labeling processes, templates, tools and systems to improve efficiency, productivity and quality and consistency across products and compliance with regulatory labeling guidance.
Associate Director - Value, Access, Insights, and Solutions 3310 Takeda Pharmaceuticals U.Associate Director - Value, Access, Insights, and SolutionsLexington, MassachusettsDevelops and maintains a broad network of mutually supportive relationships with internal Takeda colleagues (Medical Product Teams, Medical Communications, VEG, Marketing, Managed Markets, Market Access Channel Strategy, Government External Affairs, Account Management and other affiliates) to ensure US Medical scientific and outcomes research and external affairs strategies are integrated across groups. The Associate Director of Value Access Insights & Solutions is an integral member of the Marketing Content Enablement & Customer Engagement group and is responsible for: Serving as a partner to Product Medical Units, Medical Communications, Medical leads, Field Medical Leaders, Brand Teams, Market Access and Channel Strategy, Public Affairs and other Global and US internal stakeholders to ensure strategic alignment on cross-functional imperatives and initiatives.
Human Factors Engineering (HFE) Lead - Associate Engineering Fellow (AEF) 3316 Takeda Development Center AmericasHuman Factors Engineering (HFE) Lead - Associate Engineering Fellow (AEF)Lexington, MassachusettsThe HFE Lead - AEF will be integral to design and development of product user interface including hardware, software, packaging, labeling, and instruction material to support safe and effective use of the product for the intended use by the intended users in the anticipated use environment. The HFE AEF will lead the advancement of AI-enabled Human Factors Engineering capabilities across the organization by identifying and prioritizing high-impact digital transformation initiatives aligned with pipeline and platform device strategies.
Microsoft D365 CRM Or Copilot/Ai Functional Lead, Senior Associate PwCMicrosoft D365 CRM Or Copilot/Ai Functional Lead, Senior AssociateBoston, MA$77,000–$202,000 / yearPerforming key contributions to the lifecycle stages of a Dynamics 365 Solution (Assessment, Design, Development, Deployment, Testing, Operations and Diagnostics), leveraging CRM or ERP capabilities; Utilizing Microsoft BI suite, MS SQL Server and SSRS reporting services to manage the reporting lifecycle (Report Design, Creation, Publishing, Subscription, Alerts); Leveraging project management skills to lead engagements through completion while collaborating closely with the customers, technical architects, and developers; and, Utilizing effectively written and verbal business communication skills with clients and firm staff and management, emphasizing the development and delivery of presentations to business users, and use of MS Visio as a diagramming tool. Demonstrates a thorough level of abilities with, and/or a proven record of success as both an individual contributor and team member, identifying and addressing client needs: actively participating in client discussions and meetings; communicating a broad range of Firm services; and, managing engagements, including preparing concise, accurate documents and maintaining project economics while maintaining flexibility for unanticipated issues.
Associate Director, Forecast Lead, Plasma Derived Therapies 3310 Takeda Pharmaceuticals U.Associate Director, Forecast Lead, Plasma Derived TherapiesCambridge, MassachusettsRequired Skills and Qualifications: Bachelor’s degree in an analytical field such as statistics, operations research, management science, engineering, economics, business analytics, finance, mathematics, or a related field, and 8 or more years of analytics or forecasting experience; or an advanced degree in an analytical field and 6 or more years of analytics or forecasting experience. As a key member of cross-functional forecasting teams, you will develop high-quality forecasts that support annual, mid-range, and long-range planning; mid-year updates; lifecycle management; pipeline prioritization; and business case development for lifecycle management and pipeline assets.
Senior Manager or Associate Director, Feasibility Analytics & Insights Kymera TherapeuticsSenior Manager or Associate Director, Feasibility Analytics & InsightsWatertown, MA$145,000–$240,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Working in close partnership with the Director of Clinical Trial Planning and Feasibility, the individual will translate complex data into actionable insights that inform and continuously improve the accuracy and effectiveness of clinical trial planning.
Associate Director, Environmental Health & Safety ModernaTXAssociate Director, Environmental Health & SafetyNorwood, MassachusettsDemonstrated ability to use AI-enabled tools to improve EHS program execution, including development of practical use cases, prompt design, workflow creation, knowledge management, inspection readiness, event learning, risk assessment support, and generation of scalable implementation materials. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Senior Staff Software Engineer VerilySenior Staff Software EngineerRaleigh, North CarolinaOwn and drive major product and platform initiatives, leading the design and review of complex software components, systems, and features while advocating for innovative, forward-looking technical approaches that support multiple business needs. As a member and technical leader in the Consumer and Care organization, you will provide hands-on software design, development and technical leadership across a range of products and user personas to support the advancement of precision health.
Product Engineer Manufacturing--Power Line WolfSpeed Inc.Product Engineer Manufacturing--Power LineDurham, NCHere's the Gist: We are seeking an experienced and highly motivated individual to take on the challenging role of Product Quality Engineer for our growing silicon carbide Power business. This Job is Right for You if You Have (Minimum Requirements): BS in Electrical Engineering, Materials Science, Chemical Engineering, Mechanical Engineering, Physics, or related degree.
Business Quality Engineer WolfSpeed Inc.Business Quality EngineerDurham, NCThe Day-to-Day: Consult with process stakeholders, such as Operations, Quality, Sales, and Project Management, to align and draft documentation related to Product Change Notifications (PCNs) that will be delivered to our customers. This Job is Right for You if You Have (Minimum Qualifications): BS in Engineering or Technical field of study with 0-3 years of experience OR an associate's degree in quality, Business Engineering Technology, Electronics, or related technical field with 5+ years' experience.
Hardware Mechanical Engineer Hewlett Packard EnterpriseHardware Mechanical EngineerDurham, NC$66,800–$126,000 / yearDevelops and implements parameters and test plans for existing designs, including validation of tolerances, form/fit/function, shock and vibration, electromagnetic interference, safety, reliability, developing fan curves, system power measurements & acoustics. Participates as a member of project team of other mechanical hardware engineers and internal and outsourced development partners to develop reliable, cost effective and high quality solutions for low to moderately- complex products.
Mechanical Engineer The Perillo GroupMechanical EngineerCary, NCThe ideal candidate will have a strong background in mechanical engineering and be passionate about innovation and problem-solving. We are seeking a highly skilled Mechanical Engineer to join our team in Raleigh.
Generalist Engineer AGBOGeneralist EngineerRaleigh, NCThe studio's projects include Academy Award–winning Everything Everywhere All at Once, Netflix hits The Gray Man and Extraction, and Prime Video's visceral thriller The Bluff and the global Citadel franchise. As a Generalist Engineer on the Interactive team, you will contribute across multiple engineering disciplines to help build ambitious, innovative game experiences at AGBO.
Fircosoft Rule Engineer TechDigitalFircosoft Rule EngineerRaleigh, NCOnsite Fircosoft Rule Engineer 5+ years of Develop and implement Fircosoft rules to detect and flag suspicious transactions and potential violations. Troubleshoot issues and perform root cause analysis to identify and resolve problems with Fircosoft systems.
Data Loss Prevention Engineer Global Channel ManagementData Loss Prevention EngineerRaleigh, North CarolinaEngineering expertise in Data Protection this should include supporting changing the system (migrating from one DLP tool to another), standing up/turning on more functionalities at a larger scale, and understanding what the ideal future state is for growing a Data Protection program to meet the demands of a larger Bank/organization. Background can be as a strong support engineer in DLP specifically, or more general Data Protection practitioner, with oversight and engineering expertise.