Pfizer

Quality Manager

Posted Yesterday

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Seoul, KOR

Hybrid

Senior level

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

The Quality Manager establishes and implements the Quality Management System, ensuring compliance with regulatory and quality standards for pharmaceutical products, while coordinating with stakeholders and managing quality issues.

Summary Generated by Built In

Use Your Power for Purpose
The SOQ - Quality Manager will be responsible for establishing, maintaining, and implementing the Quality Management System (QMS) at the Pfizer Country Offices (PCOs) to ensure compliance with both Pfizer and Regulatory Authority expectations.
The SOQ - Quality Manager will work closely with relevant local stakeholders, such as Global Regulatory Sciences (GRS), Global Supply Chain (GSC), Medical, and PGS sites or ESOQ to ensure that the appropriate quality standards and systems are implemented and maintained for the product supply operation of the Pfizer Korea business .
The SOQ - Quality Manager will also be eligible to be named as a Responsible Person/Pharmacist (RP) (or equivalent) on the Pfizer Drug License for Wholesale.
Key Responsibilities

Act as the designated Responsible Person (RP) for imported medicinal products in Korea, ensuring ongoing compliance with MFDS, KGMP, and GDP regulatory requirements and Pfizer quality standards.
Conduct quality review and authorize market release of imported products under the PCOs importer and distribution license, confirming that all regulatory, technical, and Pfizer requirements are fully met prior to distribution and commercial supply.
Decides on the final disposition of returned, rejected, recalled or falsified products.
Manages Quarantine Alert Notifications promptly.
Coordinates and performs any market action or recall operation promptly.
Notification to Management - participates in Area Quality Review Team (AQRT) or enhance Site Quality Review Team (eSQRT) meetings as PCO representative and provide the local assessment on the subject. Contributes to AQRT or eSQRT Executive Summary for issues originating under the responsibility of the PCO. Ensure implementation of local actions identified during the AQRT or eSQRT.Serve as the primary quality liaison with local health authorities for matters related to imported product release, quality issues, supplier and logistics partner oversight, regulatory inspections, and follow‑up actions.
Ensures timely implementation of all applicable quality management systems (SOPs) within the PCO.
Assess new quality system/local regulatory requirements and adjust/enhance local systems and processes when required.
Ensures that initial and continuoustraining programs are implemented and maintained for all relevant PCO colleagues.
Ensures planned, permanent & temporary changes of GMP/GDP related activities & systems are managed & documented appropriately. Ensures change actions are completed as per agreed timelines.
Deviation Management - ensures deviations from Product Quality and Compliance requirements that occur within the responsibility of the PCO are investigated thoroughly and within required timelines.
Complaint Handling - ensures that relevant customer complaints are dealt effectively. Perform Intake, issue correspondence letter as required. Acts as a contact point for Regulatory Agency/reporter in the PCO.
Management of relevant corrective and preventative actions (CAPA).
Annual Product Quality Review (APR) - Ensure timely completion of the local MAH review of the APR.
Ensures a compliant process is in place to manage quarantine shipments.
Lead the Quality Management Review (QMR) process, ensuring systematic review of quality performance, risks, compliance status, and continual improvement actions for imported products.
Monitors key quality performance indicators on the PCOs quality performance, evaluates and highlights any significant trends and identifies actions, opportunities to propose improvements to the processes. Ensure Quality Review Meetings are conducted.
Provides on-going education on Quality to relevant PCO functional groups, to increase awareness and understanding of requirements and to enhance the Quality Culture.
Keep appropriate records of any delegated duties, if required.
Work with local cross functional team to define appropriate action plans to address the inspection/audit observation and tracks action implementation within the agreed timelines.
Lead self-inspections are performed at defined intervals following a pre-arranged program.

Quality Risk Management - ensures a program is in place for the consistent application, documentation and communication of risks to product quality/patient safety in support of GxP activities under the remit of SOQ.
Ensure the compliant management and maintenance of suppliers using the lifecycle management approach for supplier quality management.
Provide oversight of supplier and logistics partner management, including qualification, quality agreements, performance monitoring, and issue resolution, to ensure compliant manufacture, importation, storage, distribution, and supply of imported products.

Here Is What You Need (Minimum Requirements)

BA/BS with Pharmacy degree, Korean Pharmacist License is required
A minimum of 7 years in the pharmaceutical industry in a quality role.
Demonstrated ability to influence, when necessary, particularly with stakeholders and external parties.
Experience in GMP, GDP, GLP, GSP and QMS.
Technical writing and reporting.
Substantial experience in Quality market affiliates, pharmaceutical manufacturing
Familiarity with Current Good Manufacturing Practices (cGMP and KGMP) and handling compliance issues arising from cGMP deviations or product defects
Knowledge of regulations related to vendor management programs and other industry quality systems
Strong critical thinking skills and a proactive approach
Ability to collaborate effectively, manage relationships, and communicate well both in writing and verbally
Advanced computer skills in MS Office applications and a good understanding of enterprise systems such as PDM, Quality Tracking System, and Documentum platforms
Fluent in English (written & verbal),
Fluent in Korean (written & verbal)
Experience using common AI tools such as ChatGPT or Microsoft Copilot
Strong leadership and team management skills
Ability to work under pressure and meet tight deadlines
Ability to influence and negotiate with stakeholders

Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control

Skills Required

BA/BS with Pharmacy degree and Korean Pharmacist License
Minimum of 7 years in the pharmaceutical industry in a quality role
Experience in GMP, GDP, GLP, GSP and QMS
Technical writing and reporting
Substantial experience in Quality market affiliates and pharmaceutical manufacturing
Knowledge of regulations related to vendor management programs and other industry quality systems
Advanced computer skills in MS Office applications
Fluent in English and Korean
Experience using common AI tools
Strong leadership and team management skills
Ability to work under pressure and meet tight deadlines

What the Team is Saying

Pfizer Compensation & Benefits Highlights

Parental & Family Support — U.S. materials describe up to 26 weeks of parental leave (including up to 12 paid non‑medical weeks), with phased return‑to‑work plus fertility, adoption, and surrogacy financial support, backup care, lactation support, and caregiver leave. These offerings indicate depth in family‑building benefits and day‑to‑day caregiver resources.
Healthcare Strength — Core programs commonly include medical, prescription drug, dental, vision, mental‑health/EAP resources, disability insurance, preventive health programs, and free or reduced‑cost vaccinations. Voluntary Benefit Extras and wellness resources broaden coverage and access.
Retirement Support — Career pages and postings note a 401(k) with company matching plus an additional company retirement savings contribution in some plans. Company materials also reference financial‑planning education and colleague‑directed retirement funds.

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.