Associate Commercial Quality Manager

소개

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

주요업무

• Lead and oversee HSD‑related Commercial Quality activities for the Korea market, ensuring compliance with applicable regulations and quality system requirements. • Serve as the primary Commercial Quality contact for HSD and local QA-related activities in Korea. • Provide quality oversight for distribution, storage, handling, and logistics activities across the local network, including product disposition, shipment holds, and distribution-related quality decisions. • Partner with Supply Chain, Commercial, and Regulatory Affairs teams to ensure compliant product distribution and lifecycle management, and product license renewal activities, providing quality leadership and timely delivery of quality-related documentation and post-market evidence required for regulatory submissions. • Lead quality review and approval of local labeling, eIFU, and product information changes in collaboration with Regulatory Affairs. • Lead and ensure compliance with UDI management, supply record reporting, and product traceability requirements, where applicable. • Support Lead and oversee post‑market surveillance activities, including complaint handling, field action, recalls and trend analysis coordination as required. • Monitor HSD‑related quality risks, trends, and performance metrics; drive corrective and preventive actions. • Support Lead and coordinate internal audits, external audits, 3rd party audit and health authority inspections related to HSD and Commercial Quality processes. • Drive continuous improvement initiatives to strengthen compliance, consistency, and operational effectiveness.

자격요건

• Bachelor's degree in Quality, Engineering, Life Sciences, Regulatory Affairs, Supply Chain, or a related discipline (required). • Minimum 8 years of progressive experience in Quality, Regulatory Affairs, and Compliance roles, including at least 5 years of Commercial Quality experience within the Medical Device industry. • Demonstrated experience supporting distribution, logistics, or post‑market quality activities. • Strong understanding of quality system requirements and regulatory expectations for commercial operations. • Experience supporting audits, inspections, or regulatory assessments. • Ability to analyze quality risks and translate requirements into practical actions. • Language: Korean required; English proficiency preferred. • Travel: Limited; occasional domestic travel within South Korea.

우대사항

• Advanced degree in a scientific, quality, or regulatory field. • Experience in medical devices, healthcare, or other highly regulated industries. • Familiarity with Korean regulatory and distribution quality requirements. • Experience working in a multinational or matrixed organization. • Prior experience leading or coordinating HSD or Commercial Quality activities. • Quality or Regulatory certifications (e.g., ASQ, RAC). • Strong stakeholder management, communication, and problem‑solving skills.

혜택 및 복지

자세한 사항은 홈페이지 참조