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MS Solid Production Specialist Beijing

Beijing💼 Full-time🗓 2026-09-09 → 2026-09-26

Core

Execute daily production operations and quality assurance activities to manufacture medicines in compliance with GMP standards.

Role type

Associate Manager of Quality Assurance Operation (Production)

Builds

Medicines for patients

Domain

Healthcare / Pharmaceutical Manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

GMP compliance, SOP execution, Change Control, CAPA management, validation protocols, lean production, HSE systems

Preferred skills

Pharmaceutical background, continuous improvement, English communication

Technologies

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.

Seniority

Associate Manager, hands-on IC

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