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Santen

Develops medicines and devices for eye health

Assistant Quality Control Operations Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
ContractSeoul, South KoreaNo salary listedHybrid

About the Job

Requirements

  • A bachelor's degree in Pharmacy or a related scientific discipline is required.
  • A certified pharmacist license in Korea is required.
  • Proficiency in Korean is required.

Responsibilities

  • Manage quality operations for imported products, including receiving inspections, shipment release approval, import documentation, and defect investigation activities in compliance with local regulations and company standards.
  • Coordinate product testing with approved contract laboratories, ensuring timely execution, accurate documentation, and compliance with established quality requirements and specifications.
  • Oversee warehouse, storage, and distribution quality activities, including GDP/GSP compliance, environmental monitoring, inventory handling, and product disposition processes.
  • Maintain and continuously improve the local Quality Management System, including SOP management, training, deviations, CAPAs, change controls, risk assessments, quality metrics, and product quality reviews.
  • Provide quality oversight of suppliers, distributors, third-party logistics providers, and contract laboratories, ensuring effective quality agreements, compliance monitoring, and risk management.
  • Support regulatory inspections, audits, pharmacist surveillance activities, and post-market quality initiatives by maintaining inspection readiness and driving timely closure of quality actions.
  • Partner with cross-functional teams to support new product launches, technology transfers, product lifecycle changes, continuous improvement initiatives, and other business projects requiring QA/QC expertise.

Desired Qualifications

  • Proficiency in English.
  • QA/QC experience in the pharmaceutical and/or medical device industry, including GMP manufacturing and/or commercial quality operations.
  • Strong knowledge of local regulatory requirements, GMP/GDP/GSP standards, and Quality Management Systems for imported healthcare products.
  • Experience managing quality oversight of suppliers, distributors, third-party logistics providers, contract manufacturers, and external laboratories.
  • A proven track record supporting regulatory inspections, audits, pharmacist surveillance activities, and compliance-related initiatives.
  • Knowledge of PIC/S, ICH, ISO standards, cold chain management, analytical method transfer, and import/wholesale operations.

About the Company

Santen

Develops medicines and devices for eye health

Santen researches, develops, manufactures and markets medicines and medical devices for eye care. Its portfolio includes prescription treatments for glaucoma, dry eye, allergies and other eye conditions, alongside nonprescription products and surgical devices. The company combines laboratory research and clinical development with formulation, quality control and manufacturing to bring products to healthcare markets. It earns revenue from pharmaceutical and device sales, working through regional subsidiaries and commercial partners to supply healthcare professionals, pharmacies and other customers. Founded in 1890, Santen is headquartered in Osaka, Japan, and sells products internationally.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Not listed
Founded
1890

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