About Johnson Johnson
At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in in pharmaceutical, and medical devices and diagnostics markets Janssen and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
1. 포지션: QA Specialist
2. 계열사: 얀센백신 (Janssen Vaccines)
3. 근무지: 인천 송도
4. 근무 형태: Regular
[Responsibilities]
- Establishes and maintains Quality Assurance programs, procedures including batch record review and batch release
- Issue and review of Production Batch Record
- Document preparation and/or review
: Required documentation for Release (product batches, materials, utilities, facilities and area)
: Procedures/Work Instructions/Master Batch Record/Technical documents and other relevant documents
- Performs equipment release
- Performs QA oversight on the shopfloor
- Evaluates Change Controls through appropriate change impact assessments
- Performs nonconformances investigation and CAPA planning in case required
- Assists with conducting and developing site GMP trainings as a qualified trainer
- Provide active quality and compliance support and leadership to the site operational and quality units. Drive a culture of proactive quality and continuous improvement to ensure compliance with Johnson and Johnson standards, regulatory requirements, and expectations. (e.g. Internal/ health authority inspections and risk assessment, etc.)
[Requirements]
- A minimum of Bachelor’s degree is required, in life sciences or related field, such as Biology, Chemistry, Microbiology, Engineering, Pharmacy, etc.
- Fresh graduates or 1~4 years of experience in a pharmaceutical industry, preferably in sterile manufacturing environment
- Good verbal and written communication skills in English/Korean, facilitation, and presentation skills
- Good technical writing skills
- Strong organizational skills, including ability to follow tasks through to completion. Skills in prioritizing and meeting deadlines
- Word processing, presentation, spreadsheet and database skills
[지원 방법]
www.careers.jnj.com 접속 -> Position Number 2406228169W 검색 -> 해당 모집 공고의 “Apply Now” 클릭 후 온라인 지원 프로세스 진행
[제출 서류]
국문 혹은 영문 자유 양식의 이력서/자기소개서
[서류 마감일]
채용시 마감
[For more Johnson Johnson]
- JJ Linkedin: https://www.linkedin.com/company/johnson--johnson/
- JJ Corporate Page: http://www.jobkorea.co.kr/Company/1605233/Info
[유의사항]
- 국가보훈 대상자 및 장애인은 관련 서류 제출 시 관계 법령에 의거하여 우대합니다.
- 서류전형합격자에한하여개별통보합니다.단,회사사정에따라지연될수있습니다.
- 입사 지원 서류에 허위 사실이 발견될 경우, 채용 확정 이후라도 채용이 취소될 수 있으며 향후 채용이 제한됩니다.
- 제출된 서류는 반환되지 않으며, 별도 요청 시 삭제합니다.
www.careers.jnj.com
About Johnson Johnson
At Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in in pharmaceutical, and medical devices and diagnostics markets Janssen and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
1. 포지션: QA Specialist
2. 계열사: 얀센백신 (Janssen Vaccines)
3. 근무지: 인천 송도
4. 근무 형태: Regular
[Responsibilities]
- Establishes and maintains Quality Assurance programs, procedures including batch record review and batch release
- Issue and review of Production Batch Record
- Document preparation and/or review
: Required documentation for Release (product batches, materials, utilities, facilities and area)
: Procedures/Work Instructions/Master Batch Record/Technical documents and other relevant documents
- Performs equipment release
- Performs QA oversight on the shopfloor
- Evaluates Change Controls through appropriate change impact assessments
- Performs nonconformances investigation and CAPA planning in case required
- Assists with conducting and developing site GMP trainings as a qualified trainer
- Provide active quality and compliance support and leadership to the site operational and quality units. Drive a culture of proactive quality and continuous improvement to ensure compliance with Johnson and Johnson standards, regulatory requirements, and expectations. (e.g. Internal/ health authority inspections and risk assessment, etc.)
[Requirements]
- A minimum of Bachelor’s degree is required, in life sciences or related field, such as Biology, Chemistry, Microbiology, Engineering, Pharmacy, etc.
- Fresh graduates or 1~4 years of experience in a pharmaceutical industry, preferably in sterile manufacturing environment
- Good verbal and written communication skills in English/Korean, facilitation, and presentation skills
- Good technical writing skills
- Strong organizational skills, including ability to follow tasks through to completion. Skills in prioritizing and meeting deadlines
- Word processing, presentation, spreadsheet and database skills
[지원 방법]
www.careers.jnj.com 접속 -> Position Number 2406228169W 검색 -> 해당 모집 공고의 “Apply Now” 클릭 후 온라인 지원 프로세스 진행
[제출 서류]
국문 혹은 영문 자유 양식의 이력서/자기소개서
[서류 마감일]
채용시 마감
[For more Johnson Johnson]
- JJ Linkedin: https://www.linkedin.com/company/johnson--johnson/
- JJ Corporate Page: http://www.jobkorea.co.kr/Company/1605233/Info
[유의사항]
- 국가보훈 대상자 및 장애인은 관련 서류 제출 시 관계 법령에 의거하여 우대합니다.
- 서류전형합격자에한하여개별통보합니다.단,회사사정에따라지연될수있습니다.
- 입사 지원 서류에 허위 사실이 발견될 경우, 채용 확정 이후라도 채용이 취소될 수 있으며 향후 채용이 제한됩니다.
- 제출된 서류는 반환되지 않으며, 별도 요청 시 삭제합니다.
www.careers.jnj.com
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