24년 1분기 qe실 경력사원 수시채용 - Andong, 대한민국. - SK 바이오사이언스

설명

주요 업무

생산/기술
[Lead the improvement projects and or program
setting in DS/DP manufacturing Operation]
- cGMP 승인 project manage team의 manager
- Apply cGMP knowledge to drive multiple site
improvement projects and actions in the vaccine
manufacturing plant
- Manage multiple, small to medium complexity
cross-functional GMP process improvement
projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns
with the overall site QE timeline
- Serve as a project manager, tracking overall project
timeline and its elements to ensure that functional
deliverables are completed on time and according
to quality standard
- Proactively identify project risks and work with the
team and a group of SMEs to develop a
contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of
collaboration, cooperation, execution, effective
communication and cross-functional problem-
solving to enable high-performance team

[Lead the improvement projects and or program
setting in Quality Management Systems]
- cGMP 승인 project manage team의 manager
- Apply cGMP knowledge to drive multiple site
improvement projects and actions in the vaccine
manufacturing plant
- Manage multiple, small to medium complexity
cross-functional GMP process improvement
projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns
with the overall site QE timeline
- Serve as a project manager, tracking overall project
timeline and its elements to ensure that functional
deliverables are completed on time and according
to quality standard
- Proactively identify project risks and work with the
team and a group of SMEs to develop a
contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of
collaboration, cooperation, execution, effective
communication and cross-functional problem
solving to enable high-performance team

[Lead the improvement projects and or program
setting in Facilities & Equipment on site]
- cGMP 승인 project manage team의 manager
- Apply cGMP knowledge to drive multiple site
improvement projects and actions in the vaccine
manufacturing plant
- Manage multiple, small to medium complexity
cross-functional GMP process improvement
projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns
with the overall site QE timeline
- Serve as a project manager, tracking overall project
timeline and its elements to ensure that functional
deliverables are completed on time and according
to quality standard
- Proactively identify project risks and work with the
team and a group of SMEs to develop a
contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of
collaboration, cooperation, execution, effective
communication and cross-functional problem-
solving to enable high-performance team

[Lead the improvement projects and or program
setting in Laboratory Operations]
- cGMP 승인 project manage team의 manager
- Apply cGMP knowledge to drive multiple site
improvement projects and actions in the vaccine
manufacturing plant
- Manage multiple, small to medium complexity
cross-functional GMP process improvement
projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns
with the overall site QE timeline
- Serve as a project manager, tracking overall project
timeline and its elements to ensure that functional
deliverables are completed on time and according
to quality standard
- Proactively identify project risks and work with the
team and a group of SMEs to develop a
contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of
collaboration, cooperation, execution, effective
communication and cross-functional problem-
solving to enable high-performance team
○

필수
- 학력 : 학사 이상
- 경력 : 5년 이상
- 전공 : 생명공학, 생물학, 미생물학, 화학 등 유관학과
- 영어 능통자
- Must have experience in DS/DP/Aseptic processing in manufacturing operations
- Technical 영어 문서 작성 가능자
FDA/EMA 실사 대응 경험자 as an SME
- Cgmp 승인 프로세스 경험자
- Must have experience in leading projects
- Must have excellence organization and time
management skills
- Experienced with regulated GMP
environment
- Must have highly organization skills with
the ability to manage multiple tasks in
parallel
- Must have experience working with cross-
functional team

- 학력 : 학사 이상
- 경력 : 5년 이상
- 전공 : 생명공학, 생물학, 미생물학, 화학 등 유관학과
- 영어 능통자
- Must have hands on experience in Quality
Assurance (example: deviation handling/
batch release process / product complain
handling / change control process etc.)
- Technical 영어 문서 작성 가능자
- FDA/EMA 실사 대응 경험자 as an SME
- cGMP 승인 프로세스 경험자
- Must have experience in leading projects
- Must have excellence organization and time
management skills
- Experienced with regulated GMP
environment
- Must have highly organization skills with
the ability to manage multiple tasks in
parallel

- 학력 : 학사 이상
- 경력 : 5년 이상
- 전공 : 생명공학, 생물학, 미생물학, 화학 등 유관학과
- 영어 능통자
- Must have hands on experience in Facilities
& Equipment (example: HVAC, utility
equipment, DS/DP manufacturing
equipment and maintenance and calibration
program)
- Technical 영어 문서 작성 가능자
FDA/EMA 실사 대응 경험자 as an SME
- cGMP 승인 프로세스 경험자
- Must have experience in leading projects
- Must have excellence organization and time
management skills
- Experienced with regulated GMP
environment
- Must have highly organization skills with
the ability to m

우대
- Experienced in cGMP computer system management is a plus

서류 > 필기[SKCT 검사] > 면접[1차 면접] / 면접[2차 면접]

기타사항
1) 전형절차
- 서류전형 > 필기전형(SKCT검사) > 1차/2차면접 전형 > 신체검사
※ 당사 상황에 따라 1차, 2차 면접을 동시에 진행할 수 있습니다.
※ 1차 면접 종료 후 2차 면접 대상자에 대해 평판조회가 진행 됩니다.

2) 기타사항
- 국가보훈 대상자 및 장애인은 관련법에 의거 우대하여 드립니다.
- 남자의 경우 병역을 필하거나 면제의 경우 지원 가능합니다.
- 입사 후에 기재사항이 허위로 판명될 경우 입사를 취소합니다.
- 각 전형 별 합격 통보는 e-mail / SMS를 통하여 안내하므로 정확히 기재 바랍니다.
3) 지원방법
- 당사 채용사이트에서 온라인 지원만 가능합니다.

※ 유의사항
- 경력 요구 사항을 확인하시고 지원 바랍니다.
- 지원분야와 무관한 경력은 기입하지 마십시오.
- 경력사항에 아르바이트 입력은 지양해주시기 바랍니다.