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Manufacturing Division Quality Control Associate Director

JPN - Saitama - Saitama (Menuma)💼 Full-time🗓 2026-01-09 → 2026-07-31

Core

Leading a team of quality control laboratory analysts to manage quality testing for raw materials, components, finished drug substances, and final drug products, ensuring high standards of quality and compliance.

Role type

Associate Director, Quality Control (Pharmaceutical Manufacturing)

Builds

Drug substances and final drug products

Domain

Pharmaceutical manufacturing / Life Sciences

Deliverable

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

Required skills

cGMP Regulations, CAPA Management, Deviation Management, Quality Control Management, Quality Risk Management, Laboratory Information Management System (LIMS), People Leadership, Strategic Thinking, Change Management, Project Management

Preferred skills

None stated

Technologies

Laboratory Information Management System (LIMS)

Responsibilities

Ensure analytical testing activities comply with cGMP and safety requirements; lead laboratory investigations and implement corrective and preventive actions; manage the transfer of analytical methods and specifications; forecast resource needs and manage laboratory budgets; strategize and lead key Quality initiatives; manage escalations and stakeholders for operations and KPIs.

Seniority

Senior, hands-on IC with people management

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