Role Description The Executive Director, Head of Quality, Europe is responsible for leading and overseeing all Quality functions across the European region, ensuring compliance with European regulatory requirements. This role provides strategic and operational leadership across GxP Quality (GMP, GDP, GCP as applicable). In addition, this role serves as the key Quality representative for Europe, partnering closely with: - Regulatory Affairs - Manufacturing - Supply Chain - Clinical Operations - External partners Key Responsibilities: - Lead and develop the European Quality organization, ensuring alignment with global quality strategy and supporting the transition from clinical to commercial operations. - Act as the primary Quality representative for Europe, providing leadership in regional and global governance forums and serving as the main interface with European regulatory authorities (e.g., EMA, national agencies). - Ensure Quality oversight of MAH responsibilities, including lifecycle management, product complaints, recalls, and fulfillment of regulatory commitments in close collaboration with Regulatory Affairs. - Establish, implement, and maintain an effective EU Quality Management System (QMS) in compliance with EU GMP, GDP, GCP (as applicable), and ICH guidelines. - Participate in cross-functional review of Global SOPs, ensuring timely harmonization and effective implementation within the EMEA region. - Oversee key quality system processes, including deviations, CAPAs, change control, risk management, product quality complaints, and document management. - Monitor QMS performance through KPIs, risk indicators and management review process. - Review quality agreements to ensure compliance with EU GMP, GDP and other regulatory requirements across the supply chain. - Define and oversee the EU QP framework, ensuring compliant batch certification and appropriate governance of internal and/or contracted QPs. - Ensure full compliance with EU GDP requirements, including oversight of distribution activities, wholesale authorizations, and Responsible Person (RP) functions within the EU supply network. - Provide end-to-end Quality oversight of external partners (e.g., CMOs, 3PLs, distributors), including quality agreements, performance monitoring, and risk-based governance. - Lead inspection readiness across Europe and manage regulatory inspections and internal/external audits, ensuring consistent positioning and effective interaction with authorities. - Support regulatory submissions and lifecycle activities by ensuring quality oversight of relevant documentation and CMC components. - Provide Quality leadership for new product introductions, technology transfers, and commercial launches in Europe, ensuring readiness of systems, processes, and partners. - Collaborate cross-functionally with Regulatory Affairs, Technical Operations, Supply Chain, Clinical Operations, and Global Supplier Quality to ensure integrated and compliant execution across the product lifecycle. - Drive a strong, proactive quality culture across all European operations, promoting continuous improvement and accountability. Qualifications - Degree in Life Sciences, Pharmacy, Chemistry, or related field (PhD, PharmD, or MSc preferred). - 20+ years of GxP Quality experience within the pharmaceutical industry. - Track record of building and scaling Quality organizations. - Track record of working in a GMP/GDP regulated environment. - Deep knowledge of European regulatory requirements (EMA, EU GMP/GDP, ICH guidelines). Requirements - Biotech experience. - Significant leadership experience, including managing regional or global teams. Company Description Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors currently in clinical development include: - daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor - elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor - zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor - RMC-5127, a RAS(ON) G12V-selective inhibitor As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

• Serve as QA expert guiding launches, ramps, and transformation efforts ensuring adherence to established quality standards • Coordinate QA operational readiness activities, knowledge transfer, and go-live validation • Partner to design QA metrics and feedback loops to assess program effectiveness • Support business development efforts by representing CX QA sharing capabilities • Provide thought leadership influencing quality initiatives • Develop and deliver change management and communication strategies

Role Description Eaton’s IS VEH VGNA division is currently seeking a Sr. OEM Quality Specialist. This is a remote work opportunity for those living within the US/PR. The Sr. OEM Quality Specialist will plan, support, coordinate and lead activities with preparing, obtaining and sustaining customer interface and communication for the Commercial Vehicle NA region. The expected annual salary range for this role is $97,000 - $143,000 a year. Please note the salary information shown above is a general guideline only. Salaries are based upon candidate skills, experience, and qualifications, as well as market and business considerations. What you’ll do: - Develop and maintain processes that support the Customer Satisfaction and QMS interfaces with our OEM customer. - Ensure processes meet the multiple requirements of IATF16949/ISO9001, EQS and customer specifics by designing and simplifying processes to meet all requirements simultaneously. - Support improvement of key quality metrics (ZMPD PPM, Warranty, Internal PPM, PPAP on time, etc.) regionally. - Support a Six Sigma project whose scope is regional. - Support Kaizen events or BPIs where his/her expertise is required. - Eaton region primary customer contact responsible for: - Coordinate all proactive customer notifications (PPCR / PPCN / SREA / etc.). - Coordinate all PPAP submissions. - Coordinate all ZMPD/LMPD related issues. - Coordinate all 8D related issues (along with on time responsiveness). - Within OEM: Prepare and present both reactive and proactive Quality Improvement Plan presentations within region, including: - Customer scorecard reviews. - Coordinate submission of 8D’s when needed. - Support OEM PPM roadmap. - Within Eaton: Manage OEM Score Cards in order to: - Add new customers. - Ensure compliance to customer quality expectations. - Review and resolve discrepancies between OEM and Eaton Quality scorecards. - Maintain and communicate Customer Satisfaction metrics to the organization. - Prepare and host monthly scorecard reviews with cross functional team. - Support Customer Focus processes within region. - Act as a back-up when Customer Focus meeting review lead is absent. - Support Fresh Eyes audits as required. - Manage, assess, communicate and monitor changes to Customer Specific Requirements Manuals (quality, packaging, labeling, Country of Origin). - Support deployment for Change Control Process. - Lead APQP activities for New Product Launches, when applicable. - Support 3rd party audits as needed for both plant and regional locations. - Engage in Customer visits and support CSE team. Qualifications - Minimum Bachelor’s Degree from an accredited institution. - Minimum 2 years of quality experience. - Minimum 2 years of ISO9001 experience. - Minimum 2 years experience supporting 8D’s and corrective actions. Requirements - Eaton will not consider applicants for employment immigration sponsorship or support for this position. - This means that Eaton will not support any "CPT, OPT, or STEM OPT plans, F-1 to H-1B, H-1B cap registration, O-1, E-3, TN status, I-485 job portability, etc." Benefits - Eaton provides various Health and Welfare benefits as well as Retirement benefits. - Several programs that provide for paid and unpaid time away from work.

• Design, document, and execute test plans, test cases, and test scripts • Perform User Acceptance Testing (UAT) to validate business requirements and workflows • Partner with business stakeholders to clarify requirements and acceptance criteria • Identify, document, and track defects through resolution • Validate new features, enhancements, and system changes before release • Support regression testing to ensure stability across releases • Coordinate with developers and product teams to resolve issues and blockers • Facilitate or support UAT sessions with business users and SMEs • Analyze test results and provide reporting on quality and readiness • Ensure applications meet functional, usability, and data accuracy standards