• Provide scientific leadership for QC GMP activities, including method transfer, qualification, validation, and lifecycle management for drug substance (DS) and drug product (DP). • Serve as a QC subject-matter expert supporting release and stability testing, including data review, trending, and interpretation. • Lead or support investigations of deviations, OOS, and OOT results, including root cause analysis and development of corrective and preventive actions (CAPAs). • Collaborate closely with Analytical Development and CMC teams to ensure successful method transfers to QC laboratories and external CMOs. • Provide oversight of QC activities conducted at contract testing laboratories and manufacturing partners, including review of data packages and ensuring compliance with quality and regulatory requirements. • Contribute to the development and execution of control strategies for small-molecule drug substance and drug product. • Author, review, and approve QC-related documents, including methods, specifications, protocols, validation reports, and regulatory submission content. • Support regulatory inspections and audits, including preparation, response, and follow-up activities. • Identify opportunities for continuous improvement in QC processes, technologies, and compliance practices. • Mentor junior staff and serve as a technical resource across functional teams.

• Define strategy, plan, and execute tests throughout the development lifecycle • Create, maintain, and evolve documentation of test scenarios and test cases • Perform exploratory testing focused on identifying defects and risks • Analyze and interpret software requirements, ensuring the quality and consistency of deliverables • Validate and verify the implemented scope, ensuring adherence to business rules • Act critically in requirements analysis, proposing continuous improvements • Execute End-to-End (E2E) tests, ensuring full application flows function correctly • Perform API testing, validating integrations and service contracts • Collaborate with development and product teams to promote quality from conception

• Provide strategic leadership and oversight for GCP quality assurance activities supporting clinical development programs. • Lead the development, planning, and execution of GCP audits, including audits of clinical sites, CROs, vendors, and internal processes. • Own and drive regulatory inspection readiness, including preparation for FDA and other health authority inspections, inspection conduct, and response to findings. • Collaborate with Clinical Development and Clinical Operations teams to ensure studies are conducted in compliance with applicable GCP, regulatory requirements, and company SOPs. • Provide expert guidance in the identification, investigation, and resolution of quality events, including deviations, CAPAs, and audit findings. • Oversee and maintain the GCP quality systems, including processes for audit tracking, issue management, and quality metrics. • Contribute to the development, implementation, and continuous improvement of quality systems, SOPs, and policies to support GCP compliance. • Support cross-functional teams in the preparation and review of clinical documents and regulatory submissions from a quality perspective. • Manage relationships with external vendors and partners to ensure quality expectations are clearly defined and met. • Provide mentorship and guidance to junior QA staff and serve as a key quality resource across the organization.

• FUTURESEARCH is looking for a meticulous investigator to quality-check the evaluation tasks we develop for training and benchmarking frontier AI models. • You are the last check before that review. • You ask the question everyone else skipped because the answer looked reasonable. • We work against real delivery deadlines, so part of the skill is judging what deserves a deeper look.