알보젠코리아] 제조/품질관리 약사

• - Work closely to close the investigation timely manner
• - Preparation of deviation trend report

• - Review and track of CAPA and Change Control
• - Preparation of CAPA trend report

• - Receive the complaint and support root cause investigation
• - Work closely to close the investigation timely manner
• - Preparation of customer complaint trend report

• - Monitoring of production area & QC lab testing activities

• - Validation/Qualification) protocol/report
• - Batch record review
• - Preparation of Product Quality Review
• - Preparation of Common Technical Document?

• - Preparation and revision of SOPs.

• 1. A registered pharmacist in the Republic of Korea (약사면허 보유자)
• 2. Preferably more than 3 years, experience in the production and/or quality department of a pharmaceutical company. But Newcomers are acceptable.
• 3. Ability to manage multiple assignment simultaneously as part of a team.
• 4. Good interpersonal and team skills with ability to build consensus.
• 5. Highly motivated with high personal and ethical standards.
• 6. Cross-Functional collaboration for common goal

• - Batch manufacturing/packaging directions and records management (제조/포장 지시 및 기록서 관리)
• - Management and supervision of GMP standard documents compliance(GMP 기준 준수 여부 감독 및 관리)

• - Monitoring and management of manufacturing environment(제조환경 모니터링 및 관리)
• - Reviewing and approving GMP documents(GMP 문서의 검토 및 승인)

• 1. A registered pharmacist in the Republic of Korea(약사 면허 보유자)
• 2. Holding a bachelor's degree of pharmacyabove(4년제 대졸 이상, 약학 전공자)
• 3. Preferred Professional experience work experience in the production and pharmaceutical industry (제약 회사 생산 근무자 우대)
• 4. To be will acquainted with the MFDS standards and preferably also European standards on Good Manufacturing Practice(EU-GMP), as well as other international GMP standards.(MFDS 표준, EU-GMP 및 기타 국제 GMP 표준에 숙지 우대)
• 5. Good communication skill, GMP skill (원활한 커뮤니케이션 능력, GMP 지식 등)

파마메디잡