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JOB DETAILS

[KOREA] Assistant QC Operations Manager (1 year contract)

CompanySanten
LocationSeoul
Work ModeOn Site
PostedOctober 6, 2026
About The Company
As a specialized company dedicated to ophthalmology, Santen carries out research, development, marketing, and sales of pharmaceuticals, over-the-counter products, and medical devices. Santen is the market leader for prescription ophthalmic pharmaceuticals in Japan and its products now reach patients in over 60 countries and regions. With scientific knowledge and organizational capabilities nurtured over a 130-year history, Santen provides products and services to contribute to the well-being of patients, their loved ones and consequently to society. Santen Pharmaceutical Official Social Media Global Terms of Use​ https://www.santen.com/en/legal/
About the Role

Company Description

Santen is a specialized life sciences company with a proud 130-year heritage focused exclusively on ophthalmology. As a Japan-originated, global company with our footprint in over 60 countries, we are dedicated to delivering innovative treatments and digital solutions for eye health and addressing vision-related social issues for people around the world. 

As an affiliate of Santen Global, guided by our vision of “Happiness with Vision,” Santen Korea is committed to improving patients' lives through innovative eye care solutions, scientific excellence, and strong partnerships with healthcare professionals.

As we continue to expand our business, we are seeking a dedicated, passionate, and talented Assistant QC Operations Manager (1 year contract) to join our team in Korea.

Job Description

The Assistant QC Operations Manager is responsible for ensuring the quality, compliance, and integrity of Santen products throughout importation, testing, storage, release, and distribution activities in Korea. This role oversees local quality systems and quality operations, collaborates with internal and external partners including laboratories and logistics providers, supports regulatory inspections and audits, and ensures all activities are conducted in accordance with local regulatory requirements and Santen's global quality standards to maintain product quality and patient safety.

 

What you will do

  • 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 (QMS), 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 (3PLs), 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.

Qualifications

What you will bring to the role

  • Bachelor's degree in Pharmacy or a related scientific discipline
  • Must hold a certified pharmacist license in Korea.
  • Language proficiency in Korean is a must.
  • Language proficiency in English is preferred.
  • QA/QC experience in the pharmaceutical and/or medical device industry, including GMP manufacturing and/or commercial quality operations is preferred.
  • Strong knowledge of local regulatory requirements, GMP/GDP/GSP standards, and Quality Management Systems (QMS) for imported healthcare products is preferred.
  • Experience managing quality oversight of suppliers, distributors, third-party logistics providers (3PLs), contract manufacturers, and external laboratories preferred.
  • Proven track record supporting regulatory inspections, audits, pharmacist surveillance activities, and compliance-related initiatives is preferred.
  • Knowledge of PIC/S, ICH, ISO standards, cold chain management, analytical method transfer, and import/wholesale operations is an advantage is preferred.

Additional Information

Grow your career at Santen

A career at Santen is an opportunity to make a difference. Through our long-term vision outlined in Santen 2030, we are committed to be a Social Innovator - addressing the social and economic needs of people with visual impairments. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes, education and treatment. At Santen, we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment.

The Santen Group is an Equal Opportunity Employer.  We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs, role requirements and individual qualifications regardless of race, color, ethnicity, national origin/ancestry, religion, sexual orientation, gender, gender identity/ expression, age, disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

If you require any kind of accommodation during our recruitment process, please let the recruiter from our team know.

Please use the attached Resume Format template when you submit the resume.

Submit in 2 languages please. (Korean & English)

Key Skills
Quality AssuranceQuality ControlPharmacist LicenseRegulatory ComplianceGMPGDPGSPQMSSOP ManagementCAPAChange ControlRisk AssessmentSupplier ManagementAudit SupportCold Chain ManagementImport Operations
Categories
HealthcareManagement & LeadershipLogisticsScience & ResearchManufacturing
Benefits
Inclusive work environmentFlexible ways of working
Job Information
📋Core Responsibilities
The Assistant QC Operations Manager ensures the quality, compliance, and integrity of products throughout importation, testing, storage, and distribution in Korea. This role manages local quality systems, oversees supplier quality, and supports regulatory inspections to maintain product safety.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
1847
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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