[ 담당업무 ]

1. Ensure robust, efficient, and safe team operations that are compliant with cGMP and regulatory requirement.
2. Develop an effectively functioning Quality control testing team with goals and prioritization aligned with site QC.
3. Lead team staffs, guide career development, conduct performance reviews and establishing training plans. Foster collaborative team environment and high-performance culture.
4. Facilitate/ support market release, new product introductions, team/site/global projects, and continuous improvement activities to reduces costs, improve schedule adherence.
5. Review/ approve documents (raw data, log books, calibrations, SOPs, qualification/ validation protocol & reports, etc)


[ 자격조건 ]

-제약, 미생물학, 화학 전공자 선호
-7년 이상 제약업계 QC 경력자
-People managing 경력자 / 영어가능자
-local regulations, cGMPs, Quality Assurance, Audits & Regulatory Compliance, etc.에 대한 풍부한 지식



[ 전형방법 ]
1차 서류전형
2차 면접전형

[ 제출서류 ]
국문.영문이력서.경력기술서 (각종 증빙서류는 서류전형합격자에 한해 추후제출)
이메일: carly.lee@peoplework.co.kr******@*******.***
채용담당 : 이경아 전무  ( ***-****-****/ ***-****-****)

기타 유의사항

• 입사지원서 및 제출서류에 허위사실이 있을 경우 채용이 취소될 수 있습니다.