[얀센백신] Technical Launch Integrator (Technology Transfer Lead)
존슨앤드존슨
서울 용산구 한강로2가 LS용산타워 22-28F
Johnson & Johnson is the world’s most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world’s most pressing health issues.
Want to learn more about our Operating Companies?
Consumer http://www.youtube.com/watch?v=DCI7ItXYGos
Medical Devices http://www.youtube.com/watch?v=pjisNOe2oKI
Pharmacetical http://www.youtube.com/watch?v=clj_NIWV4UE
Job Description
Johnson & Johnson is the world’s most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world’s most pressing health issues.
- 포지션: Technical Launch Integrator (Technology Transfer Lead)
- 계열사: 얀센백신 (Janssen Vaccines)
- 근무지: 인천 송도
- 근무 형태: Regular
[Summary]
The Technical Launch Integrator (TLI) has overall accountability for ensuring fit for plant and commercial readiness during technical development and execution of the transfer of pharmaceutical processes and products from development into the supply chain and the global market place, as well as site-to-site transfers.
Areas of key responsibility include DS and/or DP technical support and oversight for the supply chain, planning, and execution of DS(Drug Substance) and/or DP(Drug Product) production, and manufacturing site level support of new product launch. The TLI is a member of the Manufacturing Site Operational teams, CMC Sub Team, and JSC Value Chain Team and leads the new product introduction team at the manufacturing site.
[Responsibilities]
– Technical and manufacturing integration of new and re-developed drug products from R&D (DPDS or VPAD) into the supply chain
– Contribution, review and approval of drug product technical and regulatory documents, routine technical support, integration of JSC technical expertise into project execution and QbD(Quality by Design) technical implementation at the manufacturing site level
– Single point of contact for JSC plant readiness and execution from technical transfer into commercial production including launch support
– Leading the manufacturing site team and taking the role of manufacturing site representative on the CMC Sub Team and the Value Chain Team (VCT)
– Identifying and implementing opportunities for active decrease of COGs and partnering with Development and JSC groups to develop and implement strategies to improve process robustness, fit for plant and commercialization of new products into the supply chain
-Partnering with the Technical Integrator (TI) to provide all manufacturing site related needs to the CMC Sub Team as the single point of contact at the site
– Developing the manufacturing site execution plan per product, in line with the overall strategy and plan as outlined by the CMC Sub Team and JSC VCT. The TLI will ensure alignment and endorsement of this strategy within the manufacturing site and TLI function
– Providing required manufacturing technical support, document technical input, review and approval and serving as the JSC technical expert
– Coordinating and executing product introduction at the site from transfer through launch covering raw materials, formula, process, packaging and device integration into the finished product and supporting the Value Chain Lead (VCL) for site related launch activities
– Delivering clinical through commercial product supplied by the manufacturing site, ensuring manufacturing performance, cost, and process robustness requirements are met
– Optimizing the new product introduction process, making use of JSC technology platforms, accelerating development timelines, streamlining the technical transfer process
[Requirements]
– Minimum requirements: BS/BA with experience, M.S. with experience or PhD with experience in pharmaceutical development or pharmaceutical manufacturing or related post graduate academic experience/education
– Knowledge of both pharmaceutical product R&D and Manufacturing / Technical Operations functions
– Planning and logistics skills capable of effective integration of DS and DP deliverables to support detailed execution at the manufacturing site level
– Experience with introduction of pharmaceutical products to manufacturing sites and late stage development with technical knowledge of manufacturing site unit operations
– Knowledge of manufacturing site systems and procedures; understanding of GMP requirements
– Demonstrated leadership in providing integration of activities and information across multifunctional groups and matrix teams
– Ability to foster team productivity and cohesiveness and to work collaboratively to execute, deliver and get results through the various matrix teams
– Ability to influence peers, superiors, and partners
– Motivated, self-starter able to work independently with demonstrated problem solving skills
– Fluent in written and spoken English
[지원 방법]
http://www.careers.jnj.com 접속 -> Position Number 2105966120W 검색 -> 해당 모집 공고의 “Apply Now” 클릭 후 온라인 지원 프로세스 진행
[제출 서류]
영문 자유 양식의 이력서/자기소개서
[서류 마감일]
채용시 마감
[For more J&J Korea Information]
링크드인 채용 페이지: https://www.linkedin.com/company/johnson-&-johnson/
존슨앤드존슨 채용 및 다양한 소식들을 링크드인 채용 페이지를 ‘좋아요’ 및 ‘팔로우’ 하시고 만나보시기 바랍니다.
[유의사항]
– 서류를 MS-Word 나 PDF 로 된 한 개의 파일로 미리 준비 하시기 바랍니다.
– 서류 전형 합격자에 한하여 개별 통보합니다. 단, 회사 사정에 따라 지연 될 수 있습니다.
– 온라인 접수시 “Create Your Account” 를 통해 개인 이메일 계정을 등록하신 후 온라인 지원 프로세스를 진행할 수 있습니다. Ex) G-mail/Naver/Daum 등
– 모집 분야 관련하여 자세한 내용은 J&J 홈페이지에서 확인하시기 바랍니다. http://www.careers.jnj.com
Additional Information
커리어수준 : 팀장.부장.10년이상
급여사항 : 면접 후 협의
고용형태 : 정규직
경력여부 : 경력
Guidelines for Applicants
전형방법 : 1차 서류전형-2차 면접전형
제출서류 :
영문 자유 양식의 이력서/자기소개서 (각종 증빙서류는 서류전형합격자에 한해 추후제출)
접수방법 : 홈페이지 https://www.careers.jnj.com/
마감일 : 채용시까지
The Others
- 면접은 서류전형 합격자에 개별통지 합니다.
- 국가보훈대상자와 신체장애자는 관련서류 제출시 관계법에 따라 우대함.
- 모든 서류는 반드시 MS Word로 작성하기 바랍니다.
- 제출하신 서류는 일체 반환하지 않습니다.
- 입사지원서 내용에 허위사실이 판명될 경우 입사가 취소될 수 있습니다.
- 기타 문의사항은 E-mail로 문의바랍니다.