Job title职位名称: Production Head - External Manufacturing & Supply China生产负责人 - 中国外部制造与供应 Location工作地点： Shanghai 上海 About the job工作职责 We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter –
Responsibilities: 1、Regulatory Submission Preparation & Execution Lead the preparation, review, and compilation of high-quality regulatory dossiers (e.g., CTD/eCTD format) for product registrations, variations, renewals, and other regulatory filings to NMPA and other global health authorities. Ensure
Serves as the primary point of contact for all China study activities within a global or local clinical study. In alignment with ICH-GCP, China GCP, SOPs and local regulations, the China Study Lead (CSL) partners with QSDO,
At Broadridge, weve built a culture where the highest goal is to empower others to accomplish more. If you’re passionate about developing your career, while helping others along the way, come join the Broadridge team. Role
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter –
Position Description Summary Serve as CSL’s key leader in the key innovation hubs to enhance the CSL external brand leading to BD deal flow to grow our pipeline. These senior leaders will combine ecosystem engagement, strategic scouting, and
Join us on a journey of endless possibilities At Strada, possibility isn’t just a promise – it’s the foundation of everything we do. We believe in unlocking potential for every colleague, creating a journey of growth,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Summary of Essential Functions: Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers,
Job Description 1.DC Supplier qualification and enabling, selection of suppliers for Q-programs (VDA6.3 P1 and OPL closed), and Q related release of new suppliers 2.Participation in supplier selection, Q related release during Pre-/Global Sourcing Meeting 3.Technical