올림푸스한국(주) QA Senior Manager
Tasks
The key accountability for this role is to ensure compliance of the quality management system with local Regulations and Olympus procedures covering storage, handling and distribution, complaint handling, adverse event reporting, field corrective action, audits, etc. This role provides quality leadership to safeguard product quality and patient safety through quality oversight, compliance management, and continuous improvement initiatives.
On an ongoing basis the role would be responsible for pro-active identification and assessment of risks, business continuity threats and estimation of procedural changes, resource requirements and funding required to mitigate these and representing these needs to OKR management and APAC QA leadership.
• Ensure compliance with Korean medical device regulations and Olympus procedures.
• Implement effective Quality System for OKR aligned with the Olympus Quality Management System, but defining and approving truly necessary “local variances”.
• Serve as the designated Management Representative for the QMS and facilitate management review meetings. Report performance of global quality objectives and metrics to support management review process in ensuring appropriate inputs, outputs, and follow up actions.
• Lead various QMS audits, internal/external audits, and management reviews.
• Advance company QMS through monitoring of regulations and specification changes as applicable.
• Participate in the relevant interpretation of policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
• Lead Post-Market Surveillance including customer complaint handling, reportability assessment of adverse events occurred locally and overseas and field corrective action.
• Communicate and manage cross-functional stakeholders, including OKR leadership team, Country Leader/Managing Director, business leaders and cross-functional teams, in driving overall site performance, developing and building culture of quality and continuous improvement.
• Work directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
• Drive continuous improvement - lead value-add activities, such as leading Kaizen events, facilitating pre-and post-mortems, and designing/facilitating brainstorming sessions.
• Develop and execute Quality plans to address gaps.
• Manages the development and performance of team members to support business and quality objectives.
• Drive transparent KPIs to address Quality and Compliance performance.
• Set and improve Quality Culture and Customer Focus mindset across OKR.
• Plan and manage QA department budget.
• Perform other tasks as required by the line manager.
Requirements
Education
• Bachelor’s degree in sciences or related field.
Experience
• Minimum 10 years of experience in quality management or compliance function with at least 5-7 years of management experience in a regulated environment in the MedTech industry.
• Demonstrated comprehensive expertise in the applied interpretation of relevant regulatory standards and laws applicable to the medical device industry such as: South Korean Medical Device Act, ISO, QSR, GMP, GDP.
• Demonstrated expertise in the design, implementation and measurement of quality systems and metrics.
• Experience with durable medical equipment and sterile disposable medical devices within Med Tech industry is strongly preferred.
• Initiative in innovative approaches to quality and compliance in a fast-paced changing business environment.
• Experience in data analysis, trending and presenting data in a manner to drive informed decision making.
• Ability to continuously assess the effectiveness of functional processes and to lead progressive improvement initiatives applying principles of process excellence.
• "Out of box" strategic thinker with strong leadership ability.
• As a change agent, motivated to improve organization and not be satisfied with status quo.
• Experienced in initiating, cultivating and embedding a cultural change in a complex and diverse Olympus organization.
Key Skills
• Excellent interpersonal and leadership skills with diverse cultural approach.
• A self-starter motivated and able to positively motivate others. Demonstrates the highest ethical standards, actively promotes trust, respect and integrity in all dealings both inside and outside Olympus.
• Focused, target driven with a positive, can-do attitude and a desire to improve patient experience as well as company performance.
• Excellent written and oral communication and organizational, project management skills.
• Proven analytic and problem-solving skills.
• Strong stakeholder management and ability to influence and coach others.
Information
Apply
서류전형 → 1차면접 → 온라인인성검사 → 2차면접 → 처우협의 -> 최종합격
영문이력서
* 각종 증빙서류는 서류전형합격자에 한해 추후제출
The Others
• 채용절차는 변경될 수 있으며 변경 시 사전 연락 드립니다.
• 입사지원 서류에 허위사실이 발견될 경우, 채용확정 이후라도 채용이 취소될 수 있습니다.
"우리는 모든 개인, 관점, 라이프스타일을 존중하고 공정하며 환영받는 직장을 육성하기 위해 깊이 헌신하고 있습니다. 우리는 모든 사람이 법적 기준을 완전히 준수하며 소속감을 느낄 수 있는 차별 없는 포용적인 직장 환경을 조성하는 것을 믿습니다. 공감과 단결은 회사 문화의 핵심으로, 직원들이 온전히 기여하고 번영할 수 있도록 힘을 실어줍니다. 올림푸스한국에 재능을 불어넣고자 하는 모든 분들의 지원을 진심으로 권장합니다."
Company
올림푸스한국은 소화기 내시경 및 외과용 수술장비 등을 판매하는 의료사업(Medical Business)을 영위하고 있습니다.
소화기내시경 분야 1위에 만족하지 않고 외과사업 등 각 분야로 사업 영역을 확장하여 명실상부 최고의 광학·의료기업으로 도약하고자 합니다.
- 품질경영시스템(QMS) 규제 및 Olympus 절차 준수 관리
- QMS 운영 및 로컬 예외사항 정의·승인
- QMS 관리책임자 역할 수행 및 경영검토 운영
- 내부·외부 감사 및 관리검토 주관
- 시판 후 감시, 고객 불만 처리, 이상사례 보고, 현장 시정조치 관리
- 규정 및 사양 변경 모니터링을 통한 QMS 고도화
- 품질 개선 활동 및 품질 계획 수립·실행
- 팀원 육성 및 QA 부서 예산 관리
- ✓이공계 또는 관련 학사 학위
- ✓품질관리 또는 컴플라이언스 분야 10년 이상 경력
- ✓규제 환경의 MedTech 산업 내 5~7년 이상 관리 경험
- ✓한국 의료기기법, ISO, QSR, GMP, GDP 관련 적용 및 해석 역량
- ✓품질시스템 및 지표 설계·구현·측정 경험
- ✓데이터 분석, 추세 분석 및 의사결정 지원용 데이터 प्रस्त현 경험
- ✓영문 및 국문 서면·구두 커뮤니케이션 능력
- ★내구성 의료기기 및 멸균 일회용 의료기기 경험
- ★빠르게 변화하는 사업 환경에서의 품질·컴플라이언스 혁신 경험
- ★프로세스 개선 및 지속적 개선 이니셔티브 주도 경험
- ★복잡하고 다양한 조직에서의 문화 변화 정착 경험
- ★강한 이해관계자 관리 및 코칭 역량
본 정보는 개인 구직자들의 취업지원을 위해 외국기업취업전문사이트 피플앤잡에서 수집한 정보이며, 채용회사의 사정에 따라 변경될 수 있습니다.
본 정보는 피플앤잡의 동의 및 허락 없이는 재배포 할 수 없습니다.



