CareerPlan

MS Solid Production Specialist Beijing

BeijingFull-time2026-09-09 → 2026-11-11
Based in China

Core

Associate Manager of Quality Assurance Operation ensuring production activities comply with SOP requirements and managing GMP, HSE, and lean production systems.

Role type

Senior IC Quality Assurance Specialist (Manufacturing)

Builds

Medicines for patients

Domain

Healthcare / Pharmaceutical Manufacturing

Required skills

GMP compliance, SOP development and implementation, Change Control and CAPA management, validation protocol preparation, HSE and lean production knowledge, data recording and reporting, independent execution of daily tasks

Preferred skills

Pharmaceutical degree, overseas study experience, advanced MS Office skills

Technologies

GMP, HSE, Lean Production, MS Office

Responsibilities

Execute daily production work according to SOPs, monitor production environment and processes, prepare validation protocols, implement Change Control and CAPA actions, develop and improve SOPs, report product complaints and adverse drug reactions, fill GMP documents and records

Seniority

Senior, hands-on IC