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Role overview
Job description
About Summit: Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence. Summit’s team is inspired to touch and help change lives through Summit’s clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including: Non-small Cell Lung Cancer (NSCLC) HARMONi: Phase 3 clinical study which was intended
…About this listing
- Source: Summit Therapeutics's official careers site (via Greenhouse) · last confirmed on the source 27 Oct 2026
- Posted 8 Oct 2026
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What they are looking for
Skills & requirements
Qualification
The role is responsible for ensuring that batch documentation is complete, accurate, traceable, and compliant with applicable GMP requirements, approved procedures and regulatory commitments before submission to QA for final disposition or QP certification; Coordinate the preparation and collation of batch documentation required for final batch disposition or QP certification from internal and external sources; Qualifications and Experience Essential Recognized qualification in Quality, Pharmaceutical Science, Life Sciences, Engineering or related discipline; Practical experience reviewing executed batch records and supporting batch disposition or QP certification activities
Department · Quality & RA CMC
Hiring company
Summit Therapeutics
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