Quality Auditor
- Company
- 외국계 제약회사
- Position
- Quality Auditor
- Status
- CLOSE
외국계 제약회사에서 다음과 같이 “Quality Auditor” 업무를 하실 분을 찾습니다.
*서울 근무
{RESPONSIBILITIES}
- Plan and Execute audits to the defined company standards.
- Work with the Quality and Operations and Compliance Teams to help plan audits as required.
- Make a formal Audit Report within 4 weeks of any audit, which includes recommendations.
- File audit reports in database and share internally as needed.
- Follow up on any Corrective Actions from audits and ensure they are closed out.
- Respond to queries about the state of quality in particular organizations
- Keep abreast of the requirements and the latest trends in GMP, and attend suitable training to meet those needs.
- Assist with the preparation and approval of Standard Operating Procedures (SOPs)
- Participation in the investigation of complaints related to non-compliance with quality requirements of medicines produced at a 3rd Party manufacturing facility.
{QUALIFICATIONS}
- 생물학, 약학, 화학 학사 이상 졸업한 자
- 5년 이상 경력 자, 3년 이상 제조 QA
- 제약 회사 경력 필수
- 영어 능통 자, 컴퓨터 능력 우대
- European Standards(EU-GMP, FDA, PIC/s, ISO) 등의 기준에 대한 지식 보유자
Those who are interested in this opportunity, please submit your Resume (CV) in MS Word Format by email urgently. Only qualified candidates will be contacted for interview. All resumes not contacted will be kept in DB confidentially for future positions.
KIM, Kyung Jin (Ian Kim)
CEO / Exdigm Inc.
M. 010-8722-1272
E. ceo@exdigm.com
U. www.exdigm.com
